Cargando...
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...
Gardado en:
| Publicado en: | Genet Res (Camb) |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Cambridge University Press
2015
|
| Assuntos: | |
| Acceso en liña: | 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: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|