Biochemical and genetic analysis of Leigh syndrome patients in Korea

Brain and Development

Volumn 30, Issue 6, 2008, Pages 387-390

  Chae, Jong Hee ^a,b   Lee, Jin Sook ^b   Kim, Ki Joong ^b   Hwang, Yong Seung ^b   Hirano, Michio ^a  

^a Columbia University College of Physicians and Surgeons ^*  (United States)

^b Seoul National University College of Medicine   (South Korea)

Author keywords

Biochemistry; Complex I; Leigh syndrome; Mitochondria; Molecular genetics; Mutation

Indexed keywords

CELL NUCLEUS DNA; MITOCHONDRIAL DNA;

ARTICLE; CLINICAL ARTICLE; COMPLEX I DEFICIENCY; COMPLEX III DEFICIENCY; CYTOCHROME C OXIDASE DEFICIENCY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; INFANT; LEIGH DISEASE; MALE; POINT MUTATION; PRESCHOOL CHILD; RESPIRATORY CHAIN; SOUTH KOREA;

CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; KOREA; LEIGH DISEASE; MALE; MULTIENZYME COMPLEXES; POINT MUTATION; RETROSPECTIVE STUDIES;

EID: 42649109705     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.braindev.2007.11.001     Document Type: Article

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