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OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease.

Delettre, Cécile

OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease. [electronic resource] - Molecular genetics and metabolism Feb 2002 - 97-107 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

ISSN: 1096-7192

Standard No.: 10.1006/mgme.2001.3278 doi

Subjects--Topical Terms:
Animals
Chromosomes, Human, Pair 3
GTP Phosphohydrolases--genetics
Humans
Mitochondrial Diseases--genetics
Mutation
Optic Atrophy, Autosomal Dominant--genetics
Retinal Ganglion Cells--physiology
Sequence Deletion

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