A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference47 articles.
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4. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein;Pusch;Nat Genet,2000
5. A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity;Hayakawa;Ophthalmic Paed Genet,1992
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