A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance

Molecular and Cellular Probes

Volumn 10, Issue 5, 1996, Pages 389-391

  Dumoulin, R ^a   Sagnol, I ^a   Ferlin, T ^a   Bozon, D ^a   Stepien, G ^b   Mousson, B ^a  

^a HÔPITAL DEBROUSSE   (France)

^b UNIVERSITÉ LYON 1   (France)

Author keywords

Complex III; Cytochrome b; Exercise muscle intolerance; Mitochondrial DNA; Mutation

Indexed keywords

CYTOCHROME B; MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME; MUSCLE PROTEIN; MUTANT PROTEIN; RESTRICTION ENDONUCLEASE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CONTROLLED STUDY; ENZYME DEFICIENCY; EXTRACHROMOSOMAL INHERITANCE; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; HUMAN CELL; MALE; MUSCLE DISEASE; PHENOTYPE; PRIORITY JOURNAL;

EID: 0030271757     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcpr.1996.0053     Document Type: Article

References (9)

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