Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach
Abstract Hearing loss is one of the most common birth disorders in humans, with an estimated prevalence of 1–3 in every 1000 newborns. This study investigates the molecular etiology of a hearing loss cohort using a stepwise strategy to effectively diagnose patients and address the challenges posed b...
Enregistré dans:
| Auteurs principaux: | , , , , , , , , , , |
|---|---|
| Format: | article |
| Langue: | EN |
| Publié: |
Nature Portfolio
2021
|
| Sujets: | |
| Accès en ligne: | https://doaj.org/article/5afb01c858dc4465ac1c61be42c42571 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|