Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families

BACKGROUND: Hearing loss is a rare hereditary deficit that is rather common among consanguineous populations. Autosomal recessive non-syndromic hearing loss is the predominant form of hearing loss worldwide. Although prevalent, hearing loss is extremely heterogeneous and poses a pitfall in terms of...

Descripción completa

Detalles Bibliográficos
Autores principales: Asaad, Maria, Mahfood, Mona, Al Mutery, Abdullah, Tlili, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186809/
https://www.ncbi.nlm.nih.gov/pubmed/37189200
http://dx.doi.org/10.1186/s40246-023-00489-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186809/
https://www.ncbi.nlm.nih.gov/pubmed/37189200
http://dx.doi.org/10.1186/s40246-023-00489-1

Ejemplares similares