Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

Journal of Human Genetics

Volumn 47, Issue 11, 2002, Pages 594-604

  Sudoyo, Herawati ^a   Suryadi, Helena ^a   Lertrit, Patcharee ^b   Pramoonjago, Patcharin ^a   Lyrawati, Diana ^a   Marzuki, Sangkot ^a  

^a EIJKMAN INSTITUTE FOR MOLECULAR BIOLOGY   (Indonesia)

^b MAHIDOL UNIVERSITY   (Thailand)

Author keywords

Human mtDNA; Leber's hereditary optic neuropathy; mtDNA haplotypes; mtDNA mutations; mtDNA SNP

Indexed keywords

ALANINE; ARGININE; HISTIDINE; METHIONINE; MITOCHONDRIAL DNA; THREONINE; VALINE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); RESTRICTION ENDONUCLEASE;

ARTICLE; ASIA; CONTROLLED STUDY; GENE MUTATION; GENE SEQUENCE; HAPLOTYPE; HEREDITARY OPTIC ATROPHY; HUMAN; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; PHYLOGENY; SINGLE NUCLEOTIDE POLYMORPHISM; ASIAN; CLINICAL ARTICLE; FEMALE; GENETIC ANALYSIS; GENETIC ASSOCIATION; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; MITOCHONDRIAL HAPLOGROUP; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RESTRICTION SITE; SOUTHEAST ASIAN;

EID: 0036947414     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380200091     Document Type: Article

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