The role of mtDNA background in disease expression: A new primary LHON mutation associated with Western Eurasian haplogroup J

Human Genetics

Volumn 110, Issue 2, 2002, Pages 130-138

  Brown, Michael D ^a   Starikovskaya, Elena ^b   Derbeneva, Olga ^b   Hosseini, Seyed ^a   Allen, Jon C ^a   Mikhailovskaya, Irina E ^c   Sukernik, Rem I ^b   Wallace, Douglas C ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b INSTITUTE OF CYTOLOGY AND GENETICS   (Russian Federation)

^c S FYODOROV EYE MICROSURGERY FEDERAL STATE INSTITUTION   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; MITOCHONDRIAL DNA; NUCLEOTIDE;

ADULT; ARTICLE; BASE PAIRING; BLINDNESS; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CYBRID; DATA BASE; DISEASE CARRIER; DISEASE CLASSIFICATION; DISEASE PREDISPOSITION; DISEASE TRANSMISSION; DNA SEQUENCE; GENE; GENE EXPRESSION; GENE MUTATION; GENETIC POLYMORPHISM; HAPLOTYPE; HEREDITARY OPTIC ATROPHY; HUMAN; LYMPHOBLAST; NONHUMAN; PHYLOGENY; PRIORITY JOURNAL; RISK;

AMINO ACID SEQUENCE; ANIMALS; ASIA; CELL LINE; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX I; EUROPE; FEMALE; HAPLOTYPES; HUMANS; LYMPHOCYTES; MALE; MUTATION; NADH DEHYDROGENASE; NADH, NADPH OXIDOREDUCTASES; OPTIC ATROPHY, HEREDITARY, LEBER; OXYGEN CONSUMPTION; PEDIGREE; PHYLOGENY; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 0036487995     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-001-0660-8     Document Type: Article

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