Identification of four novel variants in the CDH23 gene from four affected families with hearing loss

Background: Hearing loss (HL) is the most common form of sensory disorder in humans. Molecular diagnosis of HL is important for genetic counseling for the affected individuals and their families. Methods: To identify potential genetic causes, we performed whole-exome sequencing and related biomedica...

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Detalles Bibliográficos
Autores principales: Kang, Baoling, Lu, Xinshu, Xiong, Jianjun, Li, Yuan, Zhu, Jinwen, Cai, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713811/
https://www.ncbi.nlm.nih.gov/pubmed/36468022
http://dx.doi.org/10.3389/fgene.2022.1027396

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713811/
https://www.ncbi.nlm.nih.gov/pubmed/36468022
http://dx.doi.org/10.3389/fgene.2022.1027396

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