Utilization of amplicon-based targeted sequencing panel for the massively parallel sequencing of sporadic hearing impairment patients from Saudi Arabia

BACKGROUND: Hearing Impairment (HI) can have genetic or environmental causes and in some cases, an interplay of both. Genetic causes are difficult to determine as mutations in more than 90 genes have been shown recently to be responsible for HI. Providing a genetic diagnostic test for HI is therefor...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:BMC Med Genet
Main Authors: Dallol, Ashraf, Daghistani, Kamal, Elaimi, Aisha, Al-Wazani, Wissam A., Bamanie, Afaf, Safiah, Malek, Sagaty, Samira, Taha, Layla, Zahed, Rawabi, Bajouh, Osama, Chaudhary, Adeel Gulzar, Gari, Mamdooh Abdullah, Turki, Rola, Al-Qahtani, Mohammed Hussein, Abuzenadah, Adel Mohammed
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2016
Assuntos:
Review
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5073994/
https://ncbi.nlm.nih.gov/pubmed/27766948
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0329-8
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares