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Pathological mutations in an autosomal dominant deafness family

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NIAID Data Ecosystem2026-05-01 收录
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This study aims to identify the pathological mutation in a family of autosomal dominant nonsyndromic hearing loss. The reported deafness genes have been excluded. Exome sequencing was performed on the affected and unaffected individuals of the family.

创建时间:
2023-07-13
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