Spectrum of recurrent <i>GJB2</i> mutations in Pakistani families with autosomal recessive non-syndromic hearing loss (ARNSHL).
收藏NIAID Data Ecosystem2026-03-08 收录
数据链接：
官方服务：
资源简介：
As reference sequence NM_004004.5 was employed. EVS, exome variant server; #The pathogenicity of this mutation is controversial.
创建时间：
2014-06-20
