Molecular etiology study of hearing loss in 13 Chinese Han families

Hearing loss affecting about 2/1000 newborns is the most common congenital disease. Genetic defects caused approximately 70% of patients who have non-syndromic hearing loss. We recruited 13 Chinese Han deafness families who tested negative for GJB2, SLC26A4, and mitochondrial 12S rRNA. The probands...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Lianhua, Lin, Zhengyu, Wang, Xiaowen, Shen, Jiali, Li, Yue, Huang, Yuyu, Yang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728030/
https://www.ncbi.nlm.nih.gov/pubmed/36504663
http://dx.doi.org/10.3389/fneur.2022.1048218

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728030/
https://www.ncbi.nlm.nih.gov/pubmed/36504663
http://dx.doi.org/10.3389/fneur.2022.1048218

Ejemplares similares