Exome sequencing study of non-syndromic hereditary hearing loss. Homo sapiens
收藏NIAID Data Ecosystem2026-03-09 收录
官方服务：
资源简介：
Use of exome sequencing and high-resolution array comparative genome hybridization in families and in isolated probands for discovering novel genetic contributors to non-syndromic hereditary hearing loss.
创建时间：
2014-12-03
