Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China
Author:
Publisher
Informa UK Limited
Subject
Otorhinolaryngology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/00016489.2014.927588
Reference20 articles.
1. Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?
2. Connexin26 gene (GJB2): prevalence of mutations in the Chinese population
3. GJB2,SLC26A4and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects
4. Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss
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1. Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China;INQUIRY: The Journal of Health Care Organization, Provision, and Financing;2022-01
2. Pregestational screening of hereditary deafness genes carriers in 10,684 normal pregnant women in Zhuzhou , China;Birth Defects Research;2021-01-20
3. Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan;Human Genome Variation;2020-09-18
4. Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran;Journal of Audiology and Otology;2019-01-10
5. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China;International Journal of Pediatric Otorhinolaryngology;2018-05
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