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Original research
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability

Authors

  • Ethiraj Ravindran Institute of Cell Biology and Neurobiology, Charité Universitätsmedizin Berlin, Berlin, GermanyDepartment of Pediatric Neurology, Charité Universitätsmedizin Berlin, Berlin, GermanyCenter for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Charité – Universitätsmedizin Berlin, Berlin, Germany PubMed articlesGoogle scholar articles
  • Cynthia Gutierrez de Velazco Institute of Cell Biology and Neurobiology, Charité Universitätsmedizin Berlin, Berlin, GermanyDepartment of Pediatric Neurology, Charité Universitätsmedizin Berlin, Berlin, GermanyCenter for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Charité – Universitätsmedizin Berlin, Berlin, Germany PubMed articlesGoogle scholar articles
  • Ali Ghazanfar Department of Biotechnology, University of Azad Jammu and Kashmir, Muzaffarabad, Pakistan PubMed articlesGoogle scholar articles
  • Nadine Kraemer Institute of Cell Biology and Neurobiology, Charité Universitätsmedizin Berlin, Berlin, GermanyDepartment of Pediatric Neurology, Charité Universitätsmedizin Berlin, Berlin, GermanyCenter for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Charité – Universitätsmedizin Berlin, Berlin, Germany PubMed articlesGoogle scholar articles
  • Abdul Waheed Department of Biotechnology, University of Azad Jammu and Kashmir, Muzaffarabad, Pakistan PubMed articlesGoogle scholar articles
  • Mohsan Hanif Department of Biotechnology, University of Azad Jammu and Kashmir, Muzaffarabad, Pakistan PubMed articlesGoogle scholar articles
  • Sadia Mughal Department of Biotechnology, University of Azad Jammu and Kashmir, Muzaffarabad, Pakistan PubMed articlesGoogle scholar articles
  • Alessandro Prigione University Children’s Hospital, Department of General Pediatrics, Heinrich-Heine-Universitat Dusseldorf, Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • Na Li Laboratory of Medical Systems Biology, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China PubMed articlesGoogle scholar articles
  • Xiang Fang Laboratory of Medical Systems Biology, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China PubMed articlesGoogle scholar articles
  • Hao Hu Laboratory of Medical Systems Biology, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaGuangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaThird Affiliated Hospital of Zhengzhou University, Zhengzhou, ChinaSchool of Medicine, South China University of Technology, Guangzhou, China PubMed articlesGoogle scholar articles
  • Angela M Kaindl Institute of Cell Biology and Neurobiology, Charité Universitätsmedizin Berlin, Berlin, GermanyDepartment of Pediatric Neurology, Charité Universitätsmedizin Berlin, Berlin, GermanyCenter for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Charité – Universitätsmedizin Berlin, Berlin, Germany PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Angela M Kaindl, Institute of Cell Biology and Neurobiology, Department of Pediatric Neurology, Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Charité Universitätsmedizin Berlin, Berlin, Germany; angela.kaindl{at}charite.de
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Citation

Ravindran E, Gutierrez de Velazco C, Ghazanfar A, et al
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability

Publication history

  • Received October 27, 2020
  • Revised February 15, 2021
  • Accepted March 2, 2021
  • First published May 31, 2021.
  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

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