Lv11
40 积分 2024-06-28 加入
Characterization of a novel GRHL2 mutation reveals molecular mechanisms underlying autosomal dominant hearing loss (DFNA28): insights from structural and functional studies
32分钟前
已完结
Tmprss3 loss of function impairs cochlear inner hair cell Kcnma1 channel membrane expression
2个月前
已完结
Endocochlear potential contributes to hair cell death in TMPRSS3 hearing loss
2个月前
已完结
Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing loss
2个月前
已完结
Three ways ChatGPT helps me in my academic writing
1年前
已完结
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