Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan

OBJECTIVES: To explore the molecular epidemiology of rare deafness genes in Taiwanese sensorineural hearing impairment (SNHI) patients with cochlear implantation (CI) by performing massive parallel sequencing (MPS) and correlating genetic factors and CI outcomes. METHODS: We enrolled 41 Taiwanese no...

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Detalles Bibliográficos
Autores principales: Liu, Wei-Hsiu, Chang, Pi-Yueh, Chang, Shih-Cheng, Lu, Jang-Jih, Wu, Che-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347456/
https://www.ncbi.nlm.nih.gov/pubmed/30682115
http://dx.doi.org/10.1371/journal.pone.0211261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347456/
https://www.ncbi.nlm.nih.gov/pubmed/30682115
http://dx.doi.org/10.1371/journal.pone.0211261

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