A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency

Human Genetics

Volumn 104, Issue 6, 1999, Pages 460-466

  Valnot, Isabelle ^a   Kassis, Johanna ^a   Chretien, Dominique ^a   De Lonlay, Pascale ^a   Parfait, Béatrice ^a   Munnich, Arnold ^a   Kachaner, Jean ^a   Rustin, Pierre ^a   Rötig, Agnès ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CYTOCHROME B; MITOCHONDRIAL DNA; UBIQUINOL CYTOCHROME C REDUCTASE;

AMINO ACID SEQUENCE; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME CONFORMATION; ENZYME DEFICIENCY; ENZYME SUBUNIT; EXPRESSED SEQUENCE TAG; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERTROPHIC CARDIOMYOPATHY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0032807973     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050988     Document Type: Article

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