Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease

Biochemistry and Molecular Biology International

Volumn 38, Issue 4, 1996, Pages 693-700

  Sawano, Toni ^a   Tanakat, Masashi ^a   Ohnot, Kinji ^a   Yoneda, Makoto ^a   Ota, Yoshie ^a   Terasaki, Hiroko ^a   Awaya, Shinobu ^a   Ozawa, Takayuki ^a  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Leber's hereditary optic neuropathy; Mitochondrial DNA; Point mutation

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; GENE FREQUENCY; GENE MUTATION; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; POINT MUTATION; RNA STRUCTURE; SPECIES DIFFERENCE;

ADOLESCENT; ADULT; ANIMALS; BASE SEQUENCE; DNA, MITOCHONDRIAL; FEMALE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; OPTIC ATROPHIES, HEREDITARY; POINT MUTATION; REFERENCE VALUES; RNA, TRANSFER, GLU; RNA, TRANSFER, HIS; SEQUENCE HOMOLOGY, NUCLEIC ACID;

EID: 0029736861     PISSN: 10399712     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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