Posterior Polymorphous Corneal Dystrophy in Czech Families Maps to Chromosome 20 and Excludes theVSX1Gene-Reference-Cited by-同舟云学术

Posterior Polymorphous Corneal Dystrophy in Czech Families Maps to Chromosome 20 and Excludes theVSX1Gene

Published:2005-12-01 Issue:12 Volume:46 Page:4480
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Gwilliam Rhian¹,Liskova Petra²,Filipec Martin³,Kmoch Stanislav⁴,Jirsova Katerina³,Huckle Elizabeth J.¹,Stables Catherine L.¹,Bhattacharya Shomi S.⁵,Hardcastle Alison J.⁵,Deloukas Panos¹,Ebenezer Neil D.⁵

Affiliation:

1. From The Wellcome Trust Sanger Institute, Hinxton, United Kingdom; the

2. Division of Molecular Genetics, Institute of Ophthalmology, University College London, London, United Kingdom; the4Laboratory and Ocular Tissue Bank, Department of Ophthalmology, and the

3. Laboratory and Ocular Tissue Bank, Department of Ophthalmology, and the

4. Centre for Applied Genomics, Institute for Inherited Metabolic Disorders, Charles University, Prague, Czech Republic.

5. Division of Molecular Genetics, Institute of Ophthalmology, University College London, London, United Kingdom; the

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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