Mechanisms of disease: Mitochondrial respiratory-chain diseases

[81] TATUCH Y, 1992, AM J HUM GENET, V50, P852

[82] Respiratory chain complex I deficiency [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 106 (01): : 37 - 45

[83] Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions [J]. NATURE GENETICS, 2001, 28 (03) : 211 - 212

[84] GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 863 - 876

[85] MITOCHONDRIAL-DNA MUTATION ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY [J]. SCIENCE, 1988, 242 (4884) : 1427 - 1430

[86] The expanding spectrum of nuclear gene mutations in mitochondrial disorders [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2001, 12 (06) : 407 - 416

[81] TATUCH Y, 1992, AM J HUM GENET, V50, P852

[82] Respiratory chain complex I deficiency [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 106 (01): : 37 - 45

[83] Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions [J]. NATURE GENETICS, 2001, 28 (03) : 211 - 212

[84] GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 863 - 876

[85] MITOCHONDRIAL-DNA MUTATION ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY [J]. SCIENCE, 1988, 242 (4884) : 1427 - 1430

[86] The expanding spectrum of nuclear gene mutations in mitochondrial disorders [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2001, 12 (06) : 407 - 416