Secondary metabolic effects in complex I deficiency

Annals of Neurology

Volumn 58, Issue 4, 2005, Pages 544-552

  Esteitie, Nayla ^a   Hinttala, Reetta ^b   Wibom, Rolf ^a   Nilsson, Helene ^a   Hance, Nicole ^a   Naess, Karin ^a   Teär Fahnehjelm, Kristina ^a   Von Döbeln, Ulrika ^a   Majamaa, Kari ^b,c   Larsson, Nils Göran ^a,d  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b UNIVERSITY OF OULU   (Finland)

^c UNIVERSITY OF TURKU   (Finland)

^d KAROLINSKA INSTITUTE   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ARTICLE; CHILD; CITRIC ACID CYCLE; CLINICAL ARTICLE; CLINICAL FEATURE; COMPLEX I DEFICIENCY; FEMALE; GENE; GENE MUTATION; HUMAN; MALE; MITOCHONDRIAL RESPIRATION; MTMD4 GENE; MTND3 GENE; MUSCLE MITOCHONDRION; PATHOPHYSIOLOGY; PRIORITY JOURNAL; RESPIRATORY CHAIN; URINALYSIS;

ADENOSINE TRIPHOSPHATE; ADOLESCENT; ADULT; BLOTTING, WESTERN; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX I; FEMALE; HUMANS; INFANT; MALE; METABOLISM, INBORN ERRORS; MODELS, BIOLOGICAL; MUTATION; NADH DEHYDROGENASE; THREONINE;

EID: 25444504269     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20570     Document Type: Article

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