A novel POU domain class 3 transcription factor 4 mutation causes X-linked non-syndromic hearing loss in a Chinese family

Detalles Bibliográficos
Autores principales: Wu, Hong-Min, Jie, Hui-Qun, Wang, Hui, Wu, Ya-Qin, Chen, Zheng-Nong, Xing, Ya-Zhi, Wang, Ji-Ping, Shi, Hai-Bo, Yin, Shan-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797136/
https://www.ncbi.nlm.nih.gov/pubmed/31490266
http://dx.doi.org/10.1097/CM9.0000000000000425

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797136/
https://www.ncbi.nlm.nih.gov/pubmed/31490266
http://dx.doi.org/10.1097/CM9.0000000000000425

Ejemplares similares