No mitochondrial cytochrome oxidase (COX] gene mutations in 18 cases of COX deficiency

Human Genetics

Volumn 101, Issue 2, 1997, Pages 247-250

  Parfait, Béatrice ^a   Percheron, Agnès ^a   Chretien, Dominique ^a   Rustin, Pierre ^a   Munnich, Arnold ^a   Rötig, Agnès ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CELL NUCLEUS DNA; CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; TRANSFER RNA;

ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CYTOCHROME C OXIDASE DEFICIENCY; ENZYME ACTIVE SITE; ENZYME DEFICIENCY; ENZYME SUBUNIT; GENE MUTATION; GENE SEQUENCE; GENOME; HUMAN; HUMAN CELL; INHERITANCE; NEUROMUSCULAR DISEASE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ASSEMBLY;

CELL NUCLEUS; CYTOCHROME-C OXIDASE DEFICIENCY; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; HUMANS; MITOCHONDRIA; MITOCHONDRIAL MYOPATHIES; MUTATION; POLYMORPHISM, GENETIC;

EID: 0031441038     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050625     Document Type: Article

References (16)

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