Respiratory chain complex I deficiency

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 106, Issue 1, 2001, Pages 37-45

  Triepels, R H ^b   Van Den Heuvel, L P ^a   Trijbels, J M ^b   Smeitink, J A ^b  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b NONE

Author keywords

Complex I; Mitochondria; Mutation; OXPHOS; Ubiquinone

Indexed keywords

REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ARTICLE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MOLECULAR GENETICS; NONHUMAN; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; PRIORITY JOURNAL; RESPIRATORY CHAIN; RESPIRATORY CHAIN COMPLEX I DEFICIENCY;

CELL NUCLEUS; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX I; HUMANS; MITOCHONDRIAL DISEASES; MODELS, BIOLOGICAL; MUTATION; NADH, NADPH OXIDOREDUCTASES; OXYGEN; PHOSPHORYLATION; RNA, TRANSFER;

EID: 0034956078     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1397     Document Type: Article

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