Detection of mtDNA 11778 (G-->A) point mutation in a family with Leber's hereditary optic neuropathy by site-specific polymerase chain reaction

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

Volumn 25, Issue 2, 2003, Pages 153-155

  Niu, Shu lan ^a   Zhang, Ying ^a   Xu, Yu feng ^a   Bu, Ding fang ^a   Ren, Ze qin ^a   Wang, Shao yu ^a   Liu, Guo hua ^a   Qi, Y ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; FEMALE; GENETICS; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; METHODOLOGY; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION;

ADULT; DNA, MITOCHONDRIAL; FEMALE; HUMANS; MALE; OPTIC ATROPHY, HEREDITARY, LEBER; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION;

EID: 3042744346     PISSN: 1000503X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)