Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations

Genetic factors are an important cause of idiopathic sensorineural hearing impairment (SNHI). From the epidemiological perspective, mutations of three deafness genes: GJB2, SLC26A4, and MT-RNR1, are much more prevalent than those of other genes worldwide. However, mutation spectra of common deafness...

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Detalles Bibliográficos
Autores principales: Erdenechuluun, Jargalkhuu, Lin, Yin-Hung, Ganbat, Khongorzul, Bataakhuu, Delgermaa, Makhbal, Zaya, Tsai, Cheng-Yu, Lin, Yi-Hsin, Chan, Yen-Hui, Hsu, Chuan-Jen, Hsu, Wei-Chung, Chen, Pei-Lung, Wu, Chen-Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303056/
https://www.ncbi.nlm.nih.gov/pubmed/30576380
http://dx.doi.org/10.1371/journal.pone.0209797

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303056/
https://www.ncbi.nlm.nih.gov/pubmed/30576380
http://dx.doi.org/10.1371/journal.pone.0209797

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