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- Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness
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Letters to the editor
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Authors
- Tamar Ben-Yosef aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Marie Wattenhofer aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Saima Riazuddin aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Zubair M Ahmed aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Hamish S Scott aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Jun Kudoh aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Kazunori Shibuya aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Stylianos E Antonarakis aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Batsheva Bonne-Tamir aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Uppala Radhakrishna aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Sadaf Naz aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Zahoor Ahmed aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Sheikh Riazuddin aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Arti Pandya aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Walter E Nance aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Edward R Wilcox aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Thomas B Friedman aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Robert J Morell aLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA, bGraduate Program of Molecular and Cellular Biology, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, cCentre of Excellence in Molecular Biology, Punjab University, Lahore, Pakistan, dDivision of Medical Genetics, University of Geneva Medical School, 1 rue Michel Servet, 1211 Geneva, Switzerland, eDepartment of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan, fDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel-Aviv University, 69978 Ramat-Aviv, Israel, gDepartment of Human Genetics, Virginia Commonwealth University, Richmond 23298-0033, USA PubMed articlesGoogle scholar articles
- Dr Friedman, 5 Research Court, Room 2A-19, NIDCD/NIH, Rockville, MD 20850, USA, friedman{at}nidcd.nih.gov
Citation
Ben-Yosef T, Wattenhofer M, Riazuddin S, et al
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness
Journal of Medical Genetics 2001;38:396-400.
Publication history
- First published June 1, 2001.
Online issue publication
June 01, 2001
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Journal of Medical Genetics