Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son
Arcot Sadagopan, Karthikeyan, Battista, Robert, Keep, Rosanne B., Capasso, Jenina E., Levin, Alex V.Volume:
36
Language:
english
Journal:
Ophthalmic Genetics
DOI:
10.3109/13816810.2013.838273
Date:
June, 2015
File:
PDF, 204 KB
english, 2015