Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation

Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae

Volumn 27, Issue 1, 2005, Pages 77-80

  Zhang, Ying ^a   Wang, Zhao xia ^a   Niu, Shu lan ^a   Xu, Yu feng ^a   Pei, Pei ^a   Yuan, Yun ^a   Yang, Yan ling ^a   Qi, Y ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

LACTIC ACID; MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; ARTICLE; BLOOD; CHILD; FEMALE; GENETICS; HUMAN; INFANT; KEARNS SAYRE SYNDROME; MALE; MELAS SYNDROME; MITOCHONDRIAL ENCEPHALOMYOPATHY; MUSCLE HYPOTONIA; PHENOTYPE; POINT MUTATION; PRESCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; HUMANS; INFANT; KEARNS-SAYER SYNDROME; LACTIC ACID; MALE; MELAS SYNDROME; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUSCLE HYPOTONIA; PHENOTYPE; POINT MUTATION;

EID: 33744966165     PISSN: 1000503X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)