Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss

Hereditary hearing loss is one of the most common sensory disabilities worldwide. Mutation of POU domain class 4 transcription factor 3 (POU4F3) is considered the pathogenic cause of autosomal dominant nonsyndromic hearing loss (ADNSHL), designated as autosomal dominant nonsyndromic deafness 15. In...

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Vydáno v:Neural Plast
Hlavní autoři: Cui, Tian-Yi, Gao, Xue, Huang, Sha-Sha, Sun, Yan-Yan, Zhang, Si-Qi, Jiang, Xin-Xia, Yang, Yan-Zhong, Kang, Dong-Yang, Zhu, Qing-Wen, Yuan, Yong-Yi
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi 2020
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7349627/
https://ncbi.nlm.nih.gov/pubmed/32684921
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/6137083
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