Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

Authors

Keywords

Journal

Volume 92, Issue 1, Pages 67-75

Publisher

Elsevier BV

Online

2012-12-14

DOI

10.1016/j.ajhg.2012.10.023

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