Carregant...
A Novel Variant in SYNE4 Confirms its Causative Role in Sensorineural Hearing Loss
BACKGROUND: Hearing loss is the most common sensory deficit with many genetic and environmental underpinnings. While causative DNA variants have been identified in over 100 genes, most deafness-causing variants are rare, apart from a few exceptions. A single SYNE4 variant co-segregating with hearing...
Guardat en:
| Publicat a: | Balkan Med J |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Galenos Publishing
2018
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5863260/ https://ncbi.nlm.nih.gov/pubmed/28958982 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/balkanmedj.2017.0946 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|