TY  - GEN
AU  - Perrault,Isabelle
AU  - Hanein,Sylvain
AU  - Gerber,Sylvie
AU  - Barbet,Fabienne
AU  - Ducroq,Dominique
AU  - Dollfus,Helene
AU  - Hamel,Christian
AU  - Dufier,Jean-Louis
AU  - Munnich,Arnold
AU  - Kaplan,Josseline
AU  - Rozet,Jean-Michel
TI  - Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis
SN  - 0002-9297
PY  - 2004///1216
KW  - Alcohol Oxidoreductases
KW  - genetics
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Blindness
KW  - congenital
KW  - Chromatography, Liquid
KW  - DNA Mutational Analysis
KW  - DNA Primers
KW  - Humans
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Optic Atrophy, Hereditary, Leber
KW  - Pedigree
KW  - Sequence Alignment
N1  - Publication Type: Comparative Study; Journal Article
UR  - https://doi.org/10.1086/424889
ER  -