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Identification of novel cadherin 23 variants in a Chinese family with hearing loss

The aim of the present study was to elucidate the role of the non-syndromic autosomal recessive deafness 12 allelic variant of cadherin 23 (CDH23) in Chinese patients with non-syndromic hearing loss. The present study focused on a Chinese family with hearing loss in which there were two siblings wit...

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Detalles Bibliográficos
Autores principales:	Xu, Tianni, Zhu, Wei, Wang, Ping, Li, Haonan, Yu, Shuyuan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2019
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691240/ https://www.ncbi.nlm.nih.gov/pubmed/31322239 http://dx.doi.org/10.3892/mmr.2019.10503

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