A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness
2015 · Journal of Translational Medicine · 21 citations
https://doi.org/10.1186/s12967-015-0483-3
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Qingwen Zhu
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Qingwen Zhu is an academic researcher from Nantong University. The author has contributed to research in topics: Hearing, Cochlea, Tinnitus, Genetics & Connexins and lens biology & Vestibular and auditory disorders. The author has an h-index of 9, co-authored 23 publications.
ORCID: 0000-0003-1224-2595Papers by this author
works<scp>SNaPshot</scp> reveals high mutation and carrier frequencies of 15 common hearing loss mutants in a Chinese newborn cohort
2014 · Clinical Genetics · 9 citations
https://doi.org/10.1111/cge.12452
Additional file 1: Table S1. of A novel pore-region mutation, c.887Gâ >â A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2
2017 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.c.3726256_d1
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