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Developmental defects
Original article
Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome

Authors

  • Tawfeg Ben-Omran Section of Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Weill-Cornell Medical College, Doha, Qatar PubMed articlesGoogle scholar articles
  • Somayyeh Fahiminiya Department of Human Genetics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada McGill University and Génome Québec Innovation Centre, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Natalie Sorfazlian Department of Cell & Systems Biology, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Mariam Almuriekhi Section of Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Weill-Cornell Medical College, Doha, Qatar PubMed articlesGoogle scholar articles
  • Zafar Nawaz Cytogenetic and Molecular Cytogenetic Laboratory, Department of Laboratory, Medicine and Pathology, Hamad Medical Corporation, Doha, Qatar PubMed articlesGoogle scholar articles
  • Javad Nadaf Department of Human Genetics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada McGill University and Génome Québec Innovation Centre, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Kitam Abu Khadija Cytogenetic and Molecular Cytogenetic Laboratory, Department of Laboratory, Medicine and Pathology, Hamad Medical Corporation, Doha, Qatar PubMed articlesGoogle scholar articles
  • Samiha Zaineddin Cytogenetic and Molecular Cytogenetic Laboratory, Department of Laboratory, Medicine and Pathology, Hamad Medical Corporation, Doha, Qatar PubMed articlesGoogle scholar articles
  • Hussein Kamel Department of Radiology, Hamad Medical Corporation, Weill-Cornell Medical College, Doha, Qatar PubMed articlesGoogle scholar articles
  • Jacek Majewski Department of Human Genetics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada McGill University and Génome Québec Innovation Centre, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Vincent Tropepe Department of Cell & Systems Biology, University of Toronto, Toronto, Ontario, Canada Centre for the Analysis of Genome Evolution and Function, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Vincent Tropepe, Department of Cell & Systems Biology, University of Toronto, Toronto, Ontario, Canada M5S 3G5; v.tropepe{at}utoronto.ca
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Citation

Ben-Omran T, Fahiminiya S, Sorfazlian N, et al
Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome
Journal of Medical Genetics 2015;52:381-390.

Publication history

  • Received August 6, 2014
  • Revised March 17, 2015
  • Accepted March 22, 2015
  • First published April 14, 2015.
Online issue publication 
May 22, 2015

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