Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next‐generation sequencing

BACKGROUND: The extremely high genetic heterogeneity of hearing loss due to diverse group of genes encoding proteins required for development, function, and maintenance of the complex auditory system makes the genetic diagnosis of this disease challenging. Up to now, 121 different genes have been id...

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Detalles Bibliográficos
Autores principales: Bitarafan, Fatemeh, Seyedena, Seyed Yousef, Mahmoudi, Mahdi, Garshasbi, Masoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755797/
https://www.ncbi.nlm.nih.gov/pubmed/32864763
http://dx.doi.org/10.1002/jcla.23544

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755797/
https://www.ncbi.nlm.nih.gov/pubmed/32864763
http://dx.doi.org/10.1002/jcla.23544

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