Disease Expression in Usher Syndrome Caused byVLGR1Gene Mutation (USH2C) and Comparison withUSH2APhenotype-Reference-Cited by-同舟云学术

Disease Expression in Usher Syndrome Caused byVLGR1Gene Mutation (USH2C) and Comparison withUSH2APhenotype

Published:2005-02-01 Issue:2 Volume:46 Page:734
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Schwartz Sharon B.¹,Aleman Tomas S.¹,Cideciyan Artur V.¹,Windsor Elizabeth A. M.¹,Sumaroka Alexander¹,Roman Alejandro J.¹,Rane Tej¹,Smilko Elaine E.¹,Bennett Jean¹,Stone Edwin M.²,Kimberling William J.³,Liu Xue-Zhong⁴,Jacobson Samuel G.¹

Affiliation:

1. From the Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania; the

2. Department of Ophthalmology, Howard Hughes Medical Institute, University of Iowa Hospitals and Clinics, Iowa City, Iowa; the

3. Usher Syndrome Center, Boys Town National Research Hospital, Omaha, Nebraska; and the

4. Department of Otolaryngology, University of Miami, Miami, Florida.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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