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Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non‐syndromic hearing loss

BACKGROUND: The most common inheritance pattern responsible for congenital deafness belongs to autosomal recessive non‐syndromic hearing loss (ARNSHL) and mutations of the highly heterogeneous MYO15A locus are present in a large proportion of cases. METHODS: One Chinese family with ARNSHL was subjec...

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Detalles Bibliográficos
Autores principales:	Wang, Luming, Zhang, Yue, Xue, Qiuxia, Huang, Pinghua, Liu, Xiaodan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551133/ https://www.ncbi.nlm.nih.gov/pubmed/36217262 http://dx.doi.org/10.1002/jcla.24653

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