High incidence of GJB2 gene mutations among assortatively mating hearing impaired families in Kerala: future implications

被引:0
|
作者
AMRITKUMAR PAVITHRA
JUSTIN MARGRET JEFFREY
JAYASANKARAN CHANDRU
ARABANDI RAMESH
C. R. SRIKUMARI SRISAILAPATHY
机构
[1] University of Madras,Department of Genetics, Dr ALM Post Graduate Institute of Basic Medical Sciences
来源
Journal of Genetics | 2014年 / 93卷
关键词
mutations; connexin 26 protein; assortative mating; hearing impairment; non-complementary mating; Kerala;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:207 / 213
页数:6
相关论文
共 50 条
  • [31] Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario
    Maheshwari, M
    Vijaya, R
    Ghosh, M
    Shastri, S
    Kabra, M
    Menon, PSN
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 120A (02) : 180 - 184
  • [32] Mechanisms of congenital hearing loss caused by GJB2 gene mutations and current progress in gene therapy
    Ma, Sijie
    Chen, Xiaowan
    Wang, Yanli
    Guo, Yufen
    GENE, 2025, 946
  • [33] Overview of mutations causing early nonsyndromic hearing loss among Czech patients with excluded pathogenic mutations in GJB2 gene.
    Brozkova, D. Safka
    Markova, S. Poisson
    Lastuvkova, J.
    Raskova, D.
    Meszarosova, A. Uhrova
    Seeman, P.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 809 - 809
  • [34] Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss
    Chinetti, Viviana
    Iossa, Sandra
    Auletta, Gennaro
    Laria, Carla
    De Luca, Maria
    Di Leva, Francesca
    Riccardi, Pasquale
    Giannini, Pasquale
    Gasparini, Paolo
    Ciccodicola, Alfredo
    Marciano, Elio
    Franze, Annamaria
    INTERNATIONAL JOURNAL OF AUDIOLOGY, 2010, 49 (04) : 326 - 331
  • [35] GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China
    Shi, GZ
    Gong, LX
    Xu, XH
    Nie, WY
    Lin, Q
    Qi, YS
    HEARING RESEARCH, 2004, 197 (1-2) : 19 - 23
  • [36] Spectrum of connexin 26 gene (GJB2) mutations in families from Bashkortostan with inhereted non-syndromic hearing loss.
    Dzhemileva, LU
    Khidiatova, IM
    Khusnutdinova, EK
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 : 289 - 289
  • [37] Low frequency of GJB2 mutations in thirty-five students with hearing loss in Chinese consanguineous families
    Chen, Guanming
    Fu, Siqing
    Dong, Jiashu
    Chen, Peiwei
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2011, 75 (12) : 1535 - 1537
  • [38] Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up
    Sakata, Aki
    Kashio, Akinori
    Koyama, Misaki
    Urata, Shinji
    Koyama, Hajime
    Yamasoba, Tatsuya
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (23)
  • [39] Novel mutations of connexin 26 (GJB2) in families of non-syndromic recessive hearing loss.
    Kelley, PM
    Harris, D
    Comer, B
    Smith, SD
    Kimberling, WJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A336 - A336
  • [40] Two novel compound heterozygous families with a trimutation in the GJB2 gene causing sensorineural hearing loss
    Mirna, Martinez-Saucedo
    Maria del Refugio, Rivera-Vega
    Luz Maria, Gonzalez-Huerta
    Hector, Urueta-Cuellar
    Jaime, Toral-Lopez
    Pedro, Berruecos-Villalobos
    Sergio, Cuevas-Covarrubias
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2015, 79 (12) : 2295 - 2299