Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene-Reference-Cited by-同舟云学术

Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene

Published:2017-02-09 Issue:2 Volume:58 Page:959
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Aguirre Geoffrey K.¹,Butt Omar H.¹,Datta Ritobrato¹,Roman Alejandro J.²,Sumaroka Alexander²,Schwartz Sharon B.²,Cideciyan Artur V.²,Jacobson Samuel G.²

Affiliation:

1. Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States

2. Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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