TY  - GEN
AU  - Brown,M D
TI  - The enigmatic relationship between mitochondrial dysfunction and Leber's hereditary optic neuropathy
SN  - 0022-510X
PY  - 1999///0920
KW  - Humans
KW  - Mitochondria
KW  - physiology
KW  - Mitochondrial Encephalomyopathies
KW  - pathology
KW  - Optic Atrophies, Hereditary
N1  - Publication Type: Comment; Editorial; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1016/s0022-510x(99)00087-8
ER  -