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Mutations in TMEM231 cause Meckel–Gruber syndrome

Authors

  • Ranad Shaheen Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia PubMed articlesGoogle scholar articles
  • Shinu Ansari Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia PubMed articlesGoogle scholar articles
  • Elham AL Mardawi Department of Obstetrics and Gynecology, Security Forces Hospital, Riyadh, Saudi Arabia PubMed articlesGoogle scholar articles
  • Muneera J Alshammari Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaDepartment of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia PubMed articlesGoogle scholar articles
  • Fowzan S Alkuraya Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaDepartment of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Fowzan S Alkuraya, Developmental Genetics Unit, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyadh 11211, Saudi Arabia; falkuraya{at}kfshrc.edu.sa
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Citation

Shaheen R, Ansari S, Mardawi EA, et al
Mutations in TMEM231 cause Meckel–Gruber syndrome
Journal of Medical Genetics 2013;50:160-162.

Publication history

  • Received November 20, 2012
  • Revised December 16, 2012
  • Accepted December 17, 2012
  • First published January 24, 2013.
Online issue publication 
April 27, 2016

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