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High-throughput sequencing to decipher the genetic heterogeneity of deafness

Identifying genes causing non-syndromic hearing loss has been challenging using traditional approaches. We describe the impact that high-throughput sequencing approaches are having in discovery of genes related to hearing loss and the implications for clinical diagnosis.

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Detaylı Bibliyografya
Asıl Yazarlar: Brownstein, Zippora, Bhonker, Yoni, Avraham, Karen B
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2012
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3446284/
https://ncbi.nlm.nih.gov/pubmed/22647651
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2012-13-5-245
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