Mitochondrial DNA haplogroup Y is associated to Leigh syndrome in Chinese population

Gene

Volumn 512, Issue 2, 2013, Pages 460-463

  Hao, Xiao Dan ^a,b,e   Yang, Yan Ling ^c   Tang, Nelson Leung Sang ^e,f,g   Kong, Qing Peng ^a,e   Wu, Shi Fang ^a   Zhang, Ya Ping ^a,d,e  

^a KUNMING INSTITUTE OF ZOOLOGY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c PEKING UNIVERSITY FIRST HOSPITAL   (China)

^d YUNNAN UNIVERSITY   (China)

^e KIZ/CUHK Joint Laboratory of Bioresources and Molecular Research in Common Diseases   (China)

^f Prince of Wales Hospital   (Hong Kong)

^g CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

A10398G; Association study; Chinese population; Leigh syndrome; MtDNA haplogroup

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; HAPLOTYPE; HUMAN; LEIGH DISEASE; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL; REVERTANT; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHINA; DNA, MITOCHONDRIAL; FEMALE; HAPLOTYPES; HUMANS; INFANT; INFANT, NEWBORN; LEIGH DISEASE; MALE; MOLECULAR SEQUENCE DATA; POINT MUTATION;

EID: 84870327338     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2012.10.054     Document Type: Article

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