LACTICACIDEMIA

[91] DEFECTS IN THE E2 LIPOYL TRANSACETYLASE AND THE X-LIPOYL CONTAINING COMPONENT OF THE PYRUVATE-DEHYDROGENASE COMPLEX IN PATIENTS WITH LACTIC ACIDEMIA [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (06) : 1821 - 1824

[92] CLINICAL PRESENTATION OF MITOCHONDRIAL RESPIRATORY-CHAIN DEFECTS IN NADH-COENZYME-Q REDUCTASE AND CYTOCHROME-OXIDASE - CLUES TO PATHOGENESIS OF LEIGH DISEASE [J]. JOURNAL OF PEDIATRICS, 1987, 110 (02) : 216 - 222

[93] VARIABLE CLINICAL PRESENTATION IN PATIENTS WITH DEFECTIVE E1 COMPONENT OF PYRUVATE-DEHYDROGENASE COMPLEX [J]. JOURNAL OF PEDIATRICS, 1987, 111 (04) : 525 - 533

[94] ROBINSON BH, 1985, AM J HUM GENET, V37, P938

[95] ROCHE TE, 1989, ANN NY ACAD SCI, V573, P168, DOI 10.1111/j.1749-6632.1989.tb14994.x

[96] MITOCHONDRIAL NADH - UBIQUINONE REDUCTASE - COMPLEMENTARY-DNA SEQUENCE OF THE IMPORT PRECURSOR OF THE BOVINE 75-KDA SUBUNIT [J]. BIOCHEMISTRY, 1989, 28 (24) : 9452 - 9459

[97] SCHAPIRA AHV, 1988, LANCET, V1, P500

[98] ACCUMULATION OF THE CYTOCHROME-C OXIDASE SUBUNIT-I AND SUBUNIT-II IN YEAST REQUIRES A MITOCHONDRIAL MEMBRANE-ASSOCIATED PROTEIN, ENCODED BY THE NUCLEAR SCO1 GENE [J]. MOLECULAR & GENERAL GENETICS, 1989, 216 (01): : 37 - 43

[99] SUBACUTE NECROTIZING ENCEPHALOPATHY - OXIDATIVE-PHOSPHORYLATION DEFECTS AND THE ATPASE 6 POINT MUTATION [J]. NEUROLOGY, 1992, 42 (11) : 2168 - 2174

[100] MYOCLONIC EPILEPSY AND RAGGED-RED FIBER DISEASE (MERRF) IS ASSOCIATED WITH A MITOCHONDRIAL-DNA TRANSFER RNALYS MUTATION [J]. CELL, 1990, 61 (06) : 931 - 937

[91] DEFECTS IN THE E2 LIPOYL TRANSACETYLASE AND THE X-LIPOYL CONTAINING COMPONENT OF THE PYRUVATE-DEHYDROGENASE COMPLEX IN PATIENTS WITH LACTIC ACIDEMIA [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (06) : 1821 - 1824

[92] CLINICAL PRESENTATION OF MITOCHONDRIAL RESPIRATORY-CHAIN DEFECTS IN NADH-COENZYME-Q REDUCTASE AND CYTOCHROME-OXIDASE - CLUES TO PATHOGENESIS OF LEIGH DISEASE [J]. JOURNAL OF PEDIATRICS, 1987, 110 (02) : 216 - 222

[93] VARIABLE CLINICAL PRESENTATION IN PATIENTS WITH DEFECTIVE E1 COMPONENT OF PYRUVATE-DEHYDROGENASE COMPLEX [J]. JOURNAL OF PEDIATRICS, 1987, 111 (04) : 525 - 533

[94] ROBINSON BH, 1985, AM J HUM GENET, V37, P938

[95] ROCHE TE, 1989, ANN NY ACAD SCI, V573, P168, DOI 10.1111/j.1749-6632.1989.tb14994.x

[96] MITOCHONDRIAL NADH - UBIQUINONE REDUCTASE - COMPLEMENTARY-DNA SEQUENCE OF THE IMPORT PRECURSOR OF THE BOVINE 75-KDA SUBUNIT [J]. BIOCHEMISTRY, 1989, 28 (24) : 9452 - 9459

[97] SCHAPIRA AHV, 1988, LANCET, V1, P500

[98] ACCUMULATION OF THE CYTOCHROME-C OXIDASE SUBUNIT-I AND SUBUNIT-II IN YEAST REQUIRES A MITOCHONDRIAL MEMBRANE-ASSOCIATED PROTEIN, ENCODED BY THE NUCLEAR SCO1 GENE [J]. MOLECULAR & GENERAL GENETICS, 1989, 216 (01): : 37 - 43

[99] SUBACUTE NECROTIZING ENCEPHALOPATHY - OXIDATIVE-PHOSPHORYLATION DEFECTS AND THE ATPASE 6 POINT MUTATION [J]. NEUROLOGY, 1992, 42 (11) : 2168 - 2174

[100] MYOCLONIC EPILEPSY AND RAGGED-RED FIBER DISEASE (MERRF) IS ASSOCIATED WITH A MITOCHONDRIAL-DNA TRANSFER RNALYS MUTATION [J]. CELL, 1990, 61 (06) : 931 - 937