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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

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