Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by <i>BEST1</i> Mutations-Reference-Cited by-同舟云学术

Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 Mutations

Published:2022-12-13 Issue:13 Volume:63 Page:12
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Cideciyan Artur V.¹,Jacobson Samuel G.¹,Swider Malgorzata¹,Sumaroka Alexander¹,Sheplock Rebecca¹,Krishnan Arun K.¹,Garafalo Alexandra V.¹,Guziewicz Karina E.²,Aguirre Gustavo D.²,Beltran William A.²,Heon Elise³

Affiliation:

1. Scheie Eye Institute, Department of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States

2. Division of Experimental Retinal Therapies, Department of Clinical Sciences and Advanced Medicine, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States

3. Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Canada

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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4. Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC);Yardley;Invest Ophthalmol Vis Sci,2004

5. Variant phenotype of Best vitelliform macular dystrophy associated with compound heterozygous mutations in VMD2;Schatz;Ophthalmic Genet,2006