Report of rare and novel mutations in candidate genes in a cohort of hearing‐impaired patients

BACKGROUND: Many hearing‐impaired patients carry mutations in rare or novel genes undetected in regular genetic hot regions/genes screening. METHODS: We collected clinical and genetic data from subjects with hearing loss who visited our department for genetic counseling. Next‐generation sequencing w...

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Detalles Bibliográficos
Autores principales: Liu, Min, Liang, Yue, Huang, Bixue, Sun, Jincangjian, Chen, Kaitian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000930/
https://www.ncbi.nlm.nih.gov/pubmed/35106950
http://dx.doi.org/10.1002/mgg3.1887

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000930/
https://www.ncbi.nlm.nih.gov/pubmed/35106950
http://dx.doi.org/10.1002/mgg3.1887

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