Mitochondrial complex I deficiency in a female with multiplex arthrogryposis congenita

Pediatric Neurology

Volumn 22, Issue 1, 2000, Pages 53-56

  Vielhaber, Stefan ^a   Feistner, Helmut ^a   Schneider, Wolfgang ^b   Weis, Joachim ^c   Kunz, Wolfram S ^d  

^a Neurologische Universitatsklinik Bern   (Switzerland)

^b UNIVERSITY OF BERN   (Switzerland)

^c UNIVERSITY OF BERN   (Switzerland)

^d UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); SAPONIN;

ARTHROGRYPOSIS; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; ELECTROMYOGRAM; ENZYME DEFICIENCY; FEMALE; HISTOLOGY; HUMAN; MITOCHONDRIAL RESPIRATION; MUSCLE BIOPSY; MUSCLE METABOLISM; MYOPATHY; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; SKIN FIBROBLAST;

ARTHROGRYPOSIS; BIOPSY; CHILD; ELECTRON TRANSPORT COMPLEX I; ENERGY METABOLISM; FEMALE; HUMANS; MITOCHONDRIA; MUSCLE, SKELETAL; NADH, NADPH OXIDOREDUCTASES;

EID: 0033976915     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(99)00097-1     Document Type: Article

References (9)

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