Literature DB >> 31107121

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

Meng Zhang1,2,3,4, Yuechen Han1,2,3,4, Fengguo Zhang1,2,3,4, Xiaohui Bai1,2,3,4, Haibo Wang1,2,3,4.   

Abstract

Background: Although, half of the childhood deafness is genetically related, the molecular etiology of hearing impairment has not been demonstrated explicitly. In addition, the mutation spectrums of deafness genes vary among different areas and ethnics.
Objectives: To know more about the mutation spectrums of deafness genes in China, we tested the mutations of three common deafness genes (GJB2, SLC26A4, and mtDNA12SrRNA) in a particular deafness population from Heze area. Materials and methods: SNPscan technology was utilized to perform mutation screening for these three common deafness genes in 314 nonsyndromic deaf patients from Heze area.
Results: 38.21% (120/314) of these 314 patients with nonsyndromic hearing loss from Heze area were related to the genetic defects in these three deafness genes, including 20.06% (63/314) for GJB2, 15.29% (48/314) for SLC26A4, and 2.87% (9/314) for mtDNA12SrRNA. Furthermore, the mutation hotspots in three deaf genes were GJB2 235delC, SLC26A4 c.919-2A > G, and mtDNA12SrRNA 1555A > G, respectively, distinct from hotspots reported in other regions worldwide.
Conclusion: Our results disclosed a special and unique mutation spectrum of these three common deaf genes in Heze deaf population.

Entities:  

Keywords:  Heze area; Nonsyndromic deafness; hotspots; mutation spectrum

Year:  2019        PMID: 31107121     DOI: 10.1080/00016489.2019.1609699

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  3 in total

1.  Novel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families.

Authors:  Li-Jing Zhao; Zhi-Li Zhang; Yong Fu
Journal:  World J Clin Cases       Date:  2022-01-07       Impact factor: 1.337

2.  Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 gene.

Authors:  Chin-Ju Hu; Ying-Chang Lu; Cheng-Yu Tsai; Yen-Hui Chan; Pei-Hsuan Lin; Yi-Shan Lee; I-Shing Yu; Shu-Wha Lin; Tien-Chen Liu; Chuan-Jen Hsu; Ting-Hua Yang; Yen-Fu Cheng; Chen-Chi Wu
Journal:  Sci Rep       Date:  2021-10-25       Impact factor: 4.379

3.  Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).

Authors:  Valeriia Yu Danilchenko; Marina V Zytsar; Ekaterina A Maslova; Marita S Bady-Khoo; Nikolay A Barashkov; Igor V Morozov; Alexander A Bondar; Olga L Posukh
Journal:  Diagnostics (Basel)       Date:  2021-12-17
  3 in total

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