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Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II.
scientific article published in December 2007
Author/s
author: Jean-michel Rozet, Sylvie Gerber, Josseline Kaplan, Isabelle Perrault, Arnold Munnich, Jean-Louis Dufier, Olivier Roche, Sylvain Hanein, Nathalie Delphin
Work details
Publication date
December 1, 2007
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Language
English
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