Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: The NDUFS4 gene

Gene

Volumn 286, Issue 1, 2002, Pages 149-154

  Petruzzella, Vittoria ^a   Papa, Sergio ^a  

^a UNIVERSITY OF BARI   (Italy)

Author keywords

Leigh syndrome; Mutational analysis; NADH: ubiquinone oxidoreductase

Indexed keywords

CYCLIC AMP; GENE PRODUCT; MITOCHONDRIAL DNA; PROTEIN; PROTEIN SUBUNIT; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

CARDIOMYOPATHY; CLINICAL FEATURE; CONFERENCE PAPER; DISEASE ASSOCIATION; ENCEPHALOMYOPATHY; ENZYME ACTIVATION; ENZYME DEFICIENCY; ENZYME SUBUNIT; GENE; GENE FUNCTION; GENE MUTATION; GENE STRUCTURE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC DISORDER; HUMAN; LEIGH DISEASE; LEUKODYSTROPHY; MACROCEPHALY; MITOCHONDRIAL MEMBRANE; MITOCHONDRIAL RESPIRATION; MYOCLONUS EPILEPSY; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; OXIDATION; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID SEQUENCE; BASE SEQUENCE; CELL NUCLEUS; ELECTRON TRANSPORT COMPLEX I; HUMANS; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; MUTATION; NADH DEHYDROGENASE; NADH, NADPH OXIDOREDUCTASES; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN SUBUNITS;

EID: 0037029133     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(01)00810-1     Document Type: Conference Paper

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