Lv11
30 积分 2025-10-16 加入
Natural history and phenotype–genotype correlations in GJB2-related hearing loss: a systematic and comprehensive review
1小时前
待确认
16p11.2微缺失/微重复综合征的产前诊断
3个月前
已完结
Promotion of a new gap junction gene Cx46 (GJA3) expression in the cochlea after Cx26 (GJB2) deficiency
4个月前
已完结
Regulatory mechanisms of connexin26
4个月前
已完结
Combined AAV-mediated specific Gjb2 expression restores hearing in DFNB1 mouse models
4个月前
已完结
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