A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy.

Human mutation

Volumn 15, Issue 1, 2000, Pages 120-121

  Garcia Lozano, J R ^a   Aguilera, I ^a   Bautista, J ^a   Nunez Roldan A ^a  

^a HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOACYL TRANSFER RNA; MITOCHONDRIAL DNA; TRNA, LEUCINE; TRNA, LEUCINE-;

ARTICLE; CHROMOSOME 12; GENETICS; HEREDITARY OPTIC ATROPHY; HUMAN; MOLECULAR GENETICS; POINT MUTATION; POLYMERASE CHAIN REACTION;

CHROMOSOMES, HUMAN, PAIR 12; DNA, MITOCHONDRIAL; HUMANS; MOLECULAR SEQUENCE DATA; OPTIC ATROPHIES, HEREDITARY; POINT MUTATION; POLYMERASE CHAIN REACTION; RNA, TRANSFER, AMINO ACYL;

EID: 0033628483     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(200001)15:1<120::AID-HUMU33>3.0.CO;2-8     Document Type: Article

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