Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Published 2009 View Full Article

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Title
Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 85, Issue 5, Pages 730-736
Publisher
Elsevier BV
Online
2009-11-06
DOI
10.1016/j.ajhg.2009.10.012

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