Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss

A previous study indicated that mutations in the transmembrane protease serine 3 (TMPRSS3) gene, which encodes a transmembrane serine protease, cause nonsyndromic hearing loss (NSHL). This was the first description of a serine protease involved in hearing loss (HL). In Taiwan, however, data on the T...

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Detalles Bibliográficos
Autores principales: Wong, Swee-Hee, Yen, Yung-Chang, Li, Shuan-Yow, Yang, Jiann-Jou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177719/
https://www.ncbi.nlm.nih.gov/pubmed/32235586
http://dx.doi.org/10.3390/ijms21072382

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177719/
https://www.ncbi.nlm.nih.gov/pubmed/32235586
http://dx.doi.org/10.3390/ijms21072382

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