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...

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Dades bibliogràfiques
Publicat a:BMC Med Genet
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2016
Matèries:
Review
Accés en línia: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
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