10.1126/science.287.5454.848
10.1016/S0022-510X(98)00006-9
10.1016/S0387-7604(12)80349-4
10.1016/0022-510X(76)90063-0
10.1002/1531-8249(199906)45:6<693::AID-ANA2>3.0.CO;2-#
10.1016/0960-8966(94)00079-O
10.1016/0960-8966(91)90007-F
10.1146/annurev.biophys.27.1.329
10.1203/00006450-199011000-00027
10.1016/S0005-2728(98)00033-4
10.1126/science.283.5407.1488
Servidei S, 1996, Replacement therapy is effective in familial mitochondrial encephalomyopathy with muscle coenzyme Q10 deficiency, Neurology, 46, A420
10.1016/0165-1110(87)90028-5
10.1002/1531-8249(200005)47:5<589::AID-ANA6>3.0.CO;2-D
Teraoka M, 1999, Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency, Hum Genet, 105, 560, 10.1007/s004399900191
10.1002/1531-8249(199908)46:2<161::AID-ANA4>3.0.CO;2-O
10.1002/1531-8249(199906)45:6<787::AID-ANA13>3.0.CO;2-6
10.1016/S0092-8674(00)80611-X
10.1016/0925-4439(92)90093-3