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  • Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations

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Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations

Authors

  • Kimberly A Aldinger Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, USA PubMed articlesGoogle scholar articles
  • Nancy J Mendelsohn Medical Genetics Division, Children's Hospitals and Clinics of Minnesota, Minneapolis, Minnesota, USA Division of Genetics, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota, USA PubMed articlesGoogle scholar articles
  • Brian HY Chung Department of Paediatrics and Adolescent Medicine, Department of Obstetrics and Gynaecology, Centre for Genomic Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, Hong Kong PubMed articlesGoogle scholar articles
  • Wenjuan Zhang Department of Molecular, Cell and Developmental Biology, Department of Orthopaedic Surgery, University of California, Los Angeles, Los Angeles, California, USA PubMed articlesGoogle scholar articles
  • Daniel H Cohn Department of Molecular, Cell and Developmental Biology, Department of Orthopaedic Surgery, University of California, Los Angeles, Los Angeles, California, USA PubMed articlesGoogle scholar articles
  • Bridget Fernandez Disciplines of Genetics and Medicine, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada PubMed articlesGoogle scholar articles
  • Fowzan S Alkuraya Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia PubMed articlesGoogle scholar articles
  • William B Dobyns Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, USA Department of Pediatrics, University of Washington, Seattle, Washington, USA Department of Neurology, University of Washington, Seattle, Washington, USA PubMed articlesGoogle scholar articles
  • Cynthia J Curry Department of Pediatrics, University of California, San Francisco, San Francisco, California, USA Genetic Medicine Central California, Fresno, California, USA PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Cynthia J Curry, University of California, San Francisco/Genetic Medicine Central California, 155N Fresno St., Fresno CA 93701, USA; Cynthia.curry{at}gmail.com
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Citation

Aldinger KA, Mendelsohn NJ, Chung BH, et al
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
Journal of Medical Genetics 2016;53:427-430.

Publication history

  • Received August 20, 2015
  • Revised October 21, 2015
  • Accepted November 5, 2015
  • First published December 15, 2015.
Online issue publication 
May 24, 2016

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