TY  - GEN
AU  - Gerber,Sylvie
AU  - Hanein,Sylvain
AU  - Perrault,Isabelle
AU  - Delphin,Nathalie
AU  - Aboussair,Nisrine
AU  - Leowski,Corinne
AU  - Dufier,Jean-Louis
AU  - Roche,Olivier
AU  - Munnich,Arnold
AU  - Kaplan,Josseline
AU  - Rozet,Jean-Michel
TI  - Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II
SN  - 1098-1004
PY  - 2008///0128
KW  - DNA Mutational Analysis
KW  - Eye Proteins
KW  - genetics
KW  - Family Health
KW  - Female
KW  - Genotype
KW  - Humans
KW  - Male
KW  - Microtubule-Associated Proteins
KW  - Mutation
KW  - Optic Atrophy, Hereditary, Leber
KW  - Pedigree
KW  - Phenotype
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/humu.9513
ER  -