Mutations in LCA5 are an uncommon cause of Leber congenital...

Human Mutation 2007 Vol. 28; Iss. 12

Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II

Sylvie Gerber, Sylvain Hanein, Isabelle Perrault, Nathalie Delphin, Nisrine Aboussair, Corinne Leowski, Jean-Louis Dufier, Olivier Roche, Arnold Munnich, Josseline Kaplan, Jean-Michel Rozet
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Volume:
28
Year:
2007
Language:
english
Pages:
1
DOI:
10.1002/humu.9513
File:
PDF, 74 KB
english, 2007
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