Syndromic Choroideremia: Sublocalization of Phenotypes Associated with Martin-Probst Deafness Mental Retardation Syndrome-Reference-Cited by-同舟云学术

Syndromic Choroideremia: Sublocalization of Phenotypes Associated with Martin-Probst Deafness Mental Retardation Syndrome

Published:2008-09-01 Issue:9 Volume:49 Page:4096
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Poloschek Charlotte M.¹,Kloeckener-Gruissem Barbara²,Hansen Lutz L.¹,Bach Michael¹,Berger Wolfgang³

Affiliation:

1. From the Department of Ophthalmology, University of Freiburg, Freiburg, Germany; the

2. Division of Medical Molecular Genetics and Gene Diagnostics, Institute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland; and the4Department of Biology, ETH Zurich, Zurich, Switzerland.

3. Division of Medical Molecular Genetics and Gene Diagnostics, Institute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland; and the

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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