Mutation analysis of common GJB2 , SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health
Reference19 articles.
1. Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss
2. The genetics of deafness
3. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G,GJB2,andSLC26A4mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China
4. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India
5. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China
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1. Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China;BMC Medical Genomics;2024-02-20
2. Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China;International Journal of Pediatric Otorhinolaryngology;2024-01
3. Prevalence of TECTA and GJB2 mutations in Asian children with nonsyndromic hearing loss: A meta-analysis;Biomedical Research and Therapy;2023-06-30
4. Crucial Roles of the m.1555A>G Mutation on MT-RNR1 Gene in Hearing Loss;J BIOL REG HOMEOS AG;2022
5. Comparison of the Mutation Spectrum of Common Deafness-Causing Genes in 509 Patients With Nonsyndromic Hearing Loss in 4 Different Areas of China by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry;The Journal of International Advanced Otology;2021-12-22
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