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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...

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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

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