Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a NovelBEST1Mutation-Reference-Cited by-同舟云学术

Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a NovelBEST1Mutation

Published:2015-07-17 Issue:8 Volume:56 Page:4619
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Johnson Adiv A.¹,Bachman Lori A.¹,Gilles Benjamin J.¹,Cross Samuel D.¹,Stelzig Kimberly E.²,Resch Zachary T.²,Marmorstein Lihua Y.¹,Pulido Jose S.³,Marmorstein Alan D.¹

Affiliation:

1. Department of Ophthalmology Mayo Clinic, Rochester, Minnesota, United States

2. Center for Regenerative Medicine, Mayo Clinic, Rochester, Minnesota, United States

3. Department of Ophthalmology Mayo Clinic, Rochester, Minnesota, United States 3Department of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, United States

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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