Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province

A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct

(2017) Xiaoguang He et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Mutation analysis of common GJB2 , SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China

(2017) Jing Pan et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

The genetic basis of deafness in populations of African descent

(2017) Jason R. Rudman et al.   Journal of Genetics and Genomics

A commonSLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct

(2017) Parna Chattaraj et al.   JOURNAL OF MEDICAL GENETICS

Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran

(2017) Azim Nejatizadeh et al.   Journal of Research in Medical Sciences

A novel compound heterozygous mutation of SLC26A4 in two Chinese families with nonsyndromic hearing loss and enlarged vestibular aqueducts

(2017) Guang-Jie Zhu et al.   Molecular Medicine Reports

A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population

(2017) Siping Li et al.   PLoS One

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

(2017) Denise Yan et al.   PLoS One

The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria

(2016) Thomas Parzefall et al.   ACTA OTO-LARYNGOLOGICA

GJB2, SLC26A4, and mitochondrialDNA12S rRNAhot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China

(2016) Yalin Ma et al.   ACTA OTO-LARYNGOLOGICA

Newborn genetic screening for hearing impairment: a population-based longitudinal study

(2016) Chen-Chi Wu et al.   GENETICS IN MEDICINE

GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness

(2015) Yuan Fang et al.   CELL BIOCHEMISTRY AND BIOPHYSICS

Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India

(2015) Bidisha Adhikary et al.   GENE

Prevalence of Mutations inGJB2,SLC26A4, andmtDNAin Children with Severe or Profound Sensorineural Hearing Loss in Southwestern China

(2015) Jie Qing et al.   Genetic Testing and Molecular Biomarkers

Phenotype and genotype of deaf patients with combined genomic and mitochondrial inheritance models

(2013) Shasha Huang et al.   MITOCHONDRION

Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment

(2012) Yongyi Yuan et al.   PLoS One

Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

(2009) Pu Dai et al.   Journal of Translational Medicine

GJB2,SLC26A4and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects

(2008) Yu-Fen Guo et al.   ACTA OTO-LARYNGOLOGICA