Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency

Mitochondrial DNA

Volumn 24, Issue 1, 2013, Pages 67-73

  Ma, Yan Yan ^a   Wu, Tong Fei ^a   Liu, Yu Peng ^a   Wang, Qiao ^a   Li, Xi Yuan ^a   Zhang, Yao ^a   Song, Jin Qing ^a   Wang, Yu Jie ^a   Yang, Yan Ling ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

Leigh syndrome; Mitochondrial disorders; Respiratory chain complex I deficiency

Indexed keywords

CITRATE SYNTHASE; MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN;

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; CHINESE; COMPLEX I DEFICIENCY; DNA DETERMINATION; ENZYME ASSAY; HOSPITAL ADMISSION; HUMAN; LEIGH DISEASE; LEUKOCYTE; MALE; MITOCHONDRIAL RESPIRATORY CHAIN ENZYME ASSAY; MOTOR DYSFUNCTION; NEUROMUSCULAR DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEIZURE; WEAKNESS;

ADOLESCENT; BRAIN; CHILD; CHILD, PRESCHOOL; CHINA; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX I; HUMANS; LEIGH DISEASE; LEUKOCYTES; MAGNETIC RESONANCE IMAGING; MALE; MITOCHONDRIA; MITOCHONDRIAL DISEASES; MITOCHONDRIAL PROTEINS; NADH DEHYDROGENASE; POINT MUTATION; SEQUENCE ANALYSIS, DNA;

EID: 84872122296     PISSN: 19401736     EISSN: 19401744     Source Type: Journal    
DOI: 10.3109/19401736.2012.717932     Document Type: Article

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