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Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract

Authors

  • Wael M El-Haig Department of Ophthalmology, Zagazig University, Zagazig, Egypt PubMed articlesGoogle scholar articles
  • Cecilia Jakobsson IRO-Institute for Research in Ophthalmology, Sion, Switzerland Department of Ophthalmology, Jules-Gonin Eye Hospital, Fondation Asile des Aveugles, University of Lausanne, Lausanne, Switzerland PubMed articlesGoogle scholar articles
  • Tatiana Favez IRO-Institute for Research in Ophthalmology, Sion, Switzerland PubMed articlesGoogle scholar articles
  • Daniel F Schorderet IRO-Institute for Research in Ophthalmology, Sion, Switzerland Department of Ophthalmology, Jules-Gonin Eye Hospital, Fondation Asile des Aveugles, University of Lausanne, Lausanne, Switzerland EPFL-Faculté des Sciences du Vivant, Ecole polytechnique fédérale de Lausanne, Lausanne, Switzerland PubMed articlesGoogle scholar articles
  • Hana Abouzeid IRO-Institute for Research in Ophthalmology, Sion, Switzerland Department of Ophthalmology, Jules-Gonin Eye Hospital, Fondation Asile des Aveugles, University of Lausanne, Lausanne, Switzerland PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Hana Abouzeid, Institute for Research in Ophthalmology, Av du Grand-Champsec 64, Sion 1950, Switzerland; hana.abouzeid{at}irovision.ch
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Citation

El-Haig WM, Jakobsson C, Favez T, et al
Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract

Publication history

  • Received March 12, 2014
  • Revised May 20, 2014
  • Accepted June 21, 2014
  • First published August 4, 2014.
Online issue publication 
November 14, 2014

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