A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

BACKGROUND: Hearing loss is a clinically and genetically heterogeneous disorder. Mutations in the DFNB1 locus have been reported to be the most common cause of autosomal recessive non-syndromic hearing loss worldwide. Apart from DFNB1, many other loci and their underlying genes have also been identi...

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Główni autorzy: Imtiaz, Faiqa, Taibah, Khalid, Ramzan, Khushnooda, Bin-Khamis, Ghada, Kennedy, Shelley, Al-Mubarak, Bashayer, Trabzuni, Daniah, Allam, Rabab, Al-Mostafa, Abeer, Sogaty, Sameera, Al-Shaikh, Abdulmoneem H, Bamukhayyar, Saeed S, Meyer, Brian F, Al-Owain, Mohammed
Format: Artigo
Język:Inglês
Wydane: BioMed Central 2011
Hasła przedmiotowe:
Research Article
Dostęp online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3224387/
https://ncbi.nlm.nih.gov/pubmed/21726435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-91
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