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Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness

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Nonsyndromic hearing loss is clinically and genetically heterogeneous. In this study, we characterized the clinical features of 12 Chinese Han deaf families in which mutations in common deafness genes GJB2,… Click to show full abstract

Nonsyndromic hearing loss is clinically and genetically heterogeneous. In this study, we characterized the clinical features of 12 Chinese Han deaf families in which mutations in common deafness genes GJB2, SLC26A4, and MT‐RNR1 were excluded.

Keywords: chinese han; study; study chinese; clinical genetic; han families; genetic study

Journal Title: Molecular Genetics & Genomic Medicine
Year Published: 2020

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