High prevalence of W24X mutation in Indian families with non-syndromic deafness.

被引：0
|
作者：
Vijaya, R
Ghosh, R
Kabra, M
Menon, PSN
Deka, RC
机构：
[1] All India Inst Med Sci, Dept Pediat, Dept Otorhinolaryngol, New Delhi, India
[2] All India Inst Med Sci, Dept Otorhinolaryngol, New Delhi, India
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2002年 / 71卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2000
引用
收藏
页码：511 / 511
页数：1
相关论文
共 50 条
  • [21] GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families
    Patel, Rashmi
    Singh, Chandra Bhan
    Bhattacharya, Visweswar
    Singh, Subodh Kumar
    Ali, Akhtar
    CONGENITAL ANOMALIES, 2016, 56 (02) : 94 - 97
  • [22] Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
    Liu, XZ
    Walsh, J
    Tamagawa, Y
    Kitamura, K
    Nishizawa, M
    Steel, KP
    Brown, SDM
    NATURE GENETICS, 1997, 17 (03) : 268 - 269
  • [23] Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
    Xue-Zhong Liu
    James Walsh
    Yuya Tamagawa
    Ken Kitamura
    Masatoyo Nishizawa
    Karen P. Steel
    Steve D.M. Brown
    Nature Genetics, 1997, 17 : 268 - 269
  • [24] Deafness genes in families with non-syndromic hearing loss in Shandong, China: a genetic study
    Bai, Xiaohui
    Xu, Lei
    Zhang, Fengguo
    Xiao, Yun
    Li, Jianfeng
    Wang, Haibo
    LANCET, 2016, 388 : 80 - 80
  • [25] Molecular epidemiology of non-syndromic recessive deafness in the Indian subcontinent: the emerging spectrum.
    Ghosh, M
    Smith, T
    Vijaya, R
    Riazuddin, S
    Ahmad, ZM
    Naz, S
    Kabra, M
    Menon, PSN
    Friedman, TB
    Wilcox, ER
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 466 - 466
  • [26] Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China
    Jiang, Yi
    Huang, Shasha
    Deng, Tao
    Wu, Lihua
    Chen, Juan
    Kang, Dongyang
    Xu, Xiufeng
    Li, Ruiyu
    Han, Dongyi
    Dai, Pu
    PLOS ONE, 2015, 10 (08):
  • [27] Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness
    Riahi, Zied
    Bonnet, Crystel
    Zainine, Rim
    Louha, Malek
    Bouyacoub, Yosra
    Laroussi, Nadia
    Chargui, Mariem
    Kefi, Rym
    Jonard, Laurence
    Dorboz, Imen
    Hardelin, Jean-Pierre
    Salah, Sihem Belhaj
    Levilliers, Jacqueline
    Weil, Dominique
    McElreavey, Kenneth
    Boespflug, Odile Tanguy
    Besbes, Ghazi
    Abdelhak, Sonia
    Petit, Christine
    PLOS ONE, 2014, 9 (06):
  • [28] Neurootological findings of autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIBA gene
    Kitamura, K
    Tamagawa, Y
    Kakoi, H
    EQUILIBRIUM RESEARCH, CLINICAL EQUILIBRIOMETRY AND MODERN TREATMENT, 2000, 1201 : 674 - 674
  • [29] Evaluation of a recurrent mutation in HGF gene responsible for non-syndromic hereditary deafness in Kashmiri population
    Zaigham, Kalsoom
    Tariq, Hamna
    Qaiser, Tanveer Ahmed
    Bin Maqsood, Saad
    Khan, Asma Ali
    ADVANCEMENTS IN LIFE SCIENCES, 2020, 7 (04): : 281 - 286
  • [30] Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general gypsy population and individual subisolates
    Bouwer, Sonja
    Angelicheva, Dora
    Chandler, David
    Seeman, Pavel
    Tournev, Ivailo
    Kalaydjieva, Luba
    GENETIC TESTING, 2007, 11 (04): : 455 - 458
12345