Clinical heterogeneity in respiratory chain complex III deficiency in childhood

Journal of the Neurological Sciences

Volumn 149, Issue 1, 1997, Pages 111-117

  Mourmans, J ^a   Wendel, U ^a   Bentlage, H A C M ^a   Trijbels, J M F ^a   Smeitink, J A M ^a   De Coo, I F M ^a   Gabreels F J M ^a   Sengers, R C A ^a   Ruitenbeek, W ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

complex III; decylubiquinol:cytochrome c oxidoreductase; Fanconi syndrome; mitochondrial encephalomyopathy; respiratory chain

Indexed keywords

ARTICLE; CELL CULTURE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA DETERMINATION; ENCEPHALOMYOPATHY; FEMALE; FIBROBLAST; HUMAN; HUMAN TISSUE; INFANT; MALE; NEWBORN; PRIORITY JOURNAL; RESPIRATORY CHAIN;

ABNORMALITIES, MULTIPLE; ADENOSINE TRIPHOSPHATE; CHILD; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX III; FANCONI SYNDROME; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; LACTATES; MALE; MITOCHONDRIA, LIVER; MITOCHONDRIA, MUSCLE; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUSCLE, SKELETAL; PHOSPHOCREATINE; REFERENCE VALUES;

EID: 0031003576     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(97)05379-3     Document Type: Article

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