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The Mutation Frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of Patients with Severe to Profound Sensorineural Hearing Loss in Northwest China.

International Journal of Pediatric Otorhinolaryngology(2020)

引用 17|浏览45
关键词
Hearing loss,Genetic etiology,Targeted next-generation sequencing,Northwest China
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