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Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population

Autosomal recessive non-syndromic hearing loss (ARNSHL) is a public health concern in the Iranian population, with an incidence of 1 in 166 live births. In the present study, the whole exome sequencing (WES) method was applied to identify the mutation spectrum of NSHL patients negative for GJB2 gene...

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Detalles Bibliográficos
Autores principales:	Vallian Broojeni, Jalal, Kazemi, Arezu, Rezaei, Halimeh, Vallian, Sadeq
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2023
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414579/ https://www.ncbi.nlm.nih.gov/pubmed/37561809 http://dx.doi.org/10.1371/journal.pone.0289247

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