Loading...

Whole-exome sequencing and its impact in hereditary hearing loss

Next-generation sequencing (NGS) technologies have played a central role in the genetic revolution. These technologies, especially whole-exome sequencing, have become the primary tool of geneticists to identify the causative DNA variants in Mendelian disorders, including hereditary deafness. Current...

Full description

Saved in:
Bibliographic Details
Published in:Genet Res (Camb)
Main Authors: ATIK, TAHIR, BADEMCI, GUNEY, DIAZ-HORTA, OSCAR, BLANTON, SUSAN H., TEKIN, MUSTAFA
Format: Artigo
Language:Inglês
Published: Cambridge University Press 2015
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5503681/
https://ncbi.nlm.nih.gov/pubmed/25825321
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S001667231500004X
Tags: Add Tag
No Tags, Be the first to tag this record!