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.

Detalles Bibliográficos
Autores principales: Brownstein, Zippora, Bhonker, Yoni, Avraham, Karen B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446284/
https://www.ncbi.nlm.nih.gov/pubmed/22647651
http://dx.doi.org/10.1186/gb-2012-13-5-245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446284/
https://www.ncbi.nlm.nih.gov/pubmed/22647651
http://dx.doi.org/10.1186/gb-2012-13-5-245

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