Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees

BACKGROUND: Clinical genetic diagnosis of non-syndromic hearing loss (NSHL) is quite challenging. With regard to its high heterogeneity as well as large size of some genes, it is also really difficult to detect causative mutations using traditional approaches. One of the recent technologies called w...

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Detalles Bibliográficos
Autores principales: Khatami, Somayeh, Askari, Masomeh, Bahreini, Fatemeh, Hashemzadeh-Chaleshtori, Morteza, Hematian, Saeed, Asgharzade, Samira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672957/
https://www.ncbi.nlm.nih.gov/pubmed/33208113
http://dx.doi.org/10.1186/s12881-020-01168-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672957/
https://www.ncbi.nlm.nih.gov/pubmed/33208113
http://dx.doi.org/10.1186/s12881-020-01168-x

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