Next‐generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss

BACKGROUND: Hearing loss (HL) is a common sensory disorder in humans characterized by extreme clinical and genetic heterogeneity. In recent years, next‐generation sequencing (NGS) technologies have proven to be highly effective and powerful tools for population genetic studies of HL. Here, we analyz...

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Detalles Bibliográficos
Autores principales: Xiang, Yan‐Bao, Xu, Chen‐Yang, Xu, Yun‐Zhi, Li, Huan‐Zheng, Zhou, Li‐Li, Xu, Xue‐Qin, Chen, Zi‐Hui, Tang, Shao‐Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767562/
https://www.ncbi.nlm.nih.gov/pubmed/33095980
http://dx.doi.org/10.1002/mgg3.1539

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767562/
https://www.ncbi.nlm.nih.gov/pubmed/33095980
http://dx.doi.org/10.1002/mgg3.1539

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