Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies

Published 2015 View Full Article

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Title
Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies
Authors
Keywords
-
Journal
JAMA Ophthalmology
Volume 133, Issue 5, Pages 511
Publisher
American Medical Association (AMA)
Online
2015-02-13
DOI
10.1001/jamaophthalmol.2014.6115

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