Mutations in the X-Linked Retinitis Pigmentosa GenesRPGRandRP2Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Mutations in the X-Linked Retinitis Pigmentosa GenesRPGRandRP2Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa

Published:2013-02-19 Issue:2 Volume:54 Page:1411
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Churchill Jennifer D.¹,Bowne Sara J.¹,Sullivan Lori S.¹,Lewis Richard Alan²,Wheaton Dianna K.³,Birch David G.³,Branham Kari E.⁴,Heckenlively John R.⁴,Daiger Stephen P.¹

Affiliation:

1. From the Human Genetics Center, University of Texas Health Science Center at Houston, Houston, Texas; the

2. Department of Ophthalmology, Baylor College of Medicine, Houston, Texas;

3. The Retina Foundation of the Southwest, Dallas, Texas; and the

4. Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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