Heterogenous Point Mutations in the Mitochondrial tRNA Ser(UCN) Precursor Coexisting with the A1555G Mutation in Deaf Students from Mongolia

Samankaltaisia teoksia

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  Julkaistu: (2010)
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• Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness
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• Biochemical characterization of the mitochondrial tRNA(Ser(UCN)) T7511C mutation associated with nonsyndromic deafness
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