Pathological mutations in an autosomal dominant deafness family
收藏NIAID Data Ecosystem2026-05-01 收录
下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP449242
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资源简介：
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：
2023-07-14
