Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China

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

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

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss

(2014) Wan Du et al.   GENOMICS

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

(2013) Feng Xin et al.   Journal of Translational Medicine

Autosomal recessive nonsyndromic deafness genes: a review

(2012) Duygu Duman   Frontiers in Bioscience-Landmark

GJB2Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf

(2010) Mustafa Tekin et al.   ANNALS OF HUMAN GENETICS

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

(2010) Jianxin Lu et al.   MITOCHONDRION

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

(2009) Yongyi Yuan et al.   Journal of Translational Medicine

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

(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