Heterogenous point mutations in the mitochondrial tRNA ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia [10]

American Journal of Human Genetics

Volumn 65, Issue 6, 1999, Pages 1803-1806

  Pandya, A ^a   Xia, X J ^a   Erdenetungalag, R ^a   Amendola, M ^a   Landa, B ^a   Radnaabazar, J ^a   Dangaasuren, B ^a   Van Tuyle, G ^a   Nance, W E ^a  

^a VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL RNA; TRANSFER RNA;

AMINO ACID SUBSTITUTION; CLINICAL ARTICLE; CONTROLLED STUDY; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC HETEROGENEITY; GENETIC SCREENING; HEARING IMPAIRMENT; HUMAN; LETTER; MONGOLIA; POINT MUTATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 0033362169     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302658     Document Type: Letter

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