A South African family with the mitochondrial A1555G mutation on haplogroup L0d

Biochemical and Biophysical Research Communications

Volumn 382, Issue 2, 2009, Pages 390-394

  Human, H ^a   Lombard, D ^a   de Jong, G ^a   Bardien, S ^a  

^a STELLENBOSCH UNIVERSITY   (South Africa)

Author keywords

A1555G; Aminoglycoside induced deafness; GJB2: 35delG; Haplogroup L0d; SNaPshot technique; South African family; TRMU: A10S; tRNASer(UCN)

Indexed keywords

AMINOGLYCOSIDE; TRANSFER RNA;

ADULT; ARTICLE; BLOOD SAMPLING; CHILD; DNA MODIFICATION; FAMILY; FEMALE; GENE MUTATION; GENETIC LINKAGE; GENETIC RISK; GENETIC VARIABILITY; GENETICS; GJB2 GENE; HAPLOTYPE; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; MAJOR CLINICAL STUDY; MALE; MITOCHONDRIAL A1555G GENE; MITOCHONDRIAL GENE; MUTATION; MUTATIONAL ANALYSIS; POPULATION; PRIORITY JOURNAL; SOUTH AFRICA; TRMU GENE;

AMINOGLYCOSIDES; ANTI-BACTERIAL AGENTS; CONNEXINS; DEAFNESS; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HAPLOTYPES; HUMANS; MITOCHONDRIAL PROTEINS; MUTATION; PEDIGREE; SOUTH AFRICA; TRNA METHYLTRANSFERASES;

EID: 63349111560     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.03.032     Document Type: Article

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