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Deafness / DNA / Mitochondrial diseases / Channelopathy / Nonsyndromic deafness / MT-RNR1 / Sensorineural hearing loss / Uyghur people / GJB2 / Genetics / Biology / Philosophy of biology


Associations between GJB2, Mitochondrial 12S rRNA, SLC26A4 Mutations, and Hearing Loss among Three Ethnicities
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