TY  - GEN
AU  - Delettre,Cécile
AU  - Lenaers,Guy
AU  - Pelloquin,Laeticia
AU  - Belenguer,Pascale
AU  - Hamel,Christian P
TI  - OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease
SN  - 1096-7192
PY  - 2002///0521
KW  - Animals
KW  - Chromosomes, Human, Pair 3
KW  - GTP Phosphohydrolases
KW  - genetics
KW  - Humans
KW  - Mitochondrial Diseases
KW  - Mutation
KW  - Optic Atrophy, Autosomal Dominant
KW  - Retinal Ganglion Cells
KW  - physiology
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1006/mgme.2001.3278
ER  -