Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach

Hearing loss is one of the most common birth disorders in humans, with an estimated prevalence of 1–3 in every 1000 newborns. This study investigates the molecular etiology of a hearing loss cohort using a stepwise strategy to effectively diagnose patients and address the challenges posed by the gen...

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Detalles Bibliográficos
Autores principales: Wang, Jing, Xiang, Jiale, Chen, Lisha, Luo, Hongyu, Xu, Xiuhua, Li, Nan, Cui, Chunming, Xu, Jingjing, Song, Nana, Peng, Jiguang, Peng, Zhiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889619/
https://www.ncbi.nlm.nih.gov/pubmed/33597575
http://dx.doi.org/10.1038/s41598-021-83493-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889619/
https://www.ncbi.nlm.nih.gov/pubmed/33597575
http://dx.doi.org/10.1038/s41598-021-83493-6

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