Targeted Next-Generation Sequencing Identifies Separate Causes of Hearing Loss in One Deaf Family and Variable Clinical Manifestations for the p.R161C Mutation in SOX10

Copyright © 2020 Xiaoyu Yu et al.

Détails bibliographiques
Publié dans:Neural plasticity. - 1998. - 2020(2020) vom: 15., Seite 8860837
Auteur principal: Yu, Xiaoyu (Auteur)
Autres auteurs: Lin, Yun, Wu, Hao
Format: Article en ligne
Langue:English
Publié: 2020
Accès à la collection:Neural plasticity
Sujets:Journal Article Research Support, Non-U.S. Gov't GJB2 protein, human SOX10 protein, human SOXE Transcription Factors Connexin 26 127120-53-0