GJB2 mutations in Indian families with Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss (ARNSHL).

被引：0
|
作者：
Vijaya, R
Kabra, M
Menon, PSN
Deka, RC
机构：
[1] All India Inst Med Sci, Dept Otorhinolaryngol, New Delhi, India
[2] All India Inst Med Sci, Dept Pediat, Genet Unit, New Delhi, India
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05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：
2199
引用
收藏
页码：544 / 544
页数：1
相关论文
共 50 条
  • [41] Genetic study of autosomal recessive nonsyndromic sensorineural hearing loss in Kuwaiti children
    Farid A.S.
    Shabana M.I.
    Selim M.H.
    Al Sebeih K.H.
    Abdulla M.M.
    [J]. The Egyptian Journal of Otolaryngology, 2012, 28 (1) : 35 - 43
  • [42] Connexin mutation testing of children with nonsyndromic, autosomal recessive sensorineural hearing loss
    Thomas, MA
    Der Kaloustian, VM
    Tewfik, TL
    [J]. JOURNAL OF OTOLARYNGOLOGY, 2004, 33 (03): : 189 - 192
  • [43] Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss
    Kelley, PM
    Harris, DJ
    Comer, BC
    Askew, JW
    Fowler, T
    Smith, SD
    Kimberling, WJ
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (04) : 792 - 799
  • [44] GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder
    Xia, Hong
    Huang, Xiangjun
    Xu, Hongbo
    Zhou, Yong-an
    Gong, Lina
    Yang, Zhijian
    Lv, Jingyan
    Deng, Hao
    [J]. GENETICS AND MOLECULAR BIOLOGY, 2019, 42 (01) : 48 - 51
  • [45] De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing loss
    Huang, Shasha
    Yuan, Yongyi
    Liu, Jun
    Han, Dongyi
    Kang, Dongyang
    Zhang, Xin
    Dong, Min
    Yan, Xiaofei
    Dai, Pu
    [J]. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2011, 75 (10) : 1333 - 1336
  • [46] Mutation Analysis of GJB2 and GJB6 Genes and Screening of Nine Common DFNB Loci in Iranian Pedigrees with Autosomal Recessive Nonsyndromic Hearing Loss
    Azadegan-Dehkordi, Fatemeh
    Koohiyan, Mahbobeh
    Shirzad, Maryam
    Bahrami, Tayyeb
    Yazdanpanahi, Nasrin
    Tabatabaiefar, Mohammad Amin
    Pourpaknia, Reza
    Farrokhi, Effat
    Hashemzadeh-Chaleshtori, Morteza
    [J]. INDIAN JOURNAL OF OTOLOGY, 2019, 25 (02) : 97 - 102
  • [47] TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss
    Saba Battelino
    Gasper Klancar
    Jernej Kovac
    Tadej Battelino
    Katarina Trebusak Podkrajsek
    [J]. European Archives of Oto-Rhino-Laryngology, 2016, 273 : 1151 - 1154
  • [48] TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss
    Battelino, Saba
    Klancar, Gasper
    Kovac, Jernej
    Battelino, Tadej
    Podkrajsek, Katarina Trebusak
    [J]. EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2016, 273 (05) : 1151 - 1154
  • [49] A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)
    Lench, NJ
    Markham, AF
    Mueller, RF
    Kelsell, DP
    Smith, RJH
    Willems, PJ
    Schatteman, I
    Capon, H
    Van De Heyning, PJ
    Van Camp, G
    [J]. JOURNAL OF MEDICAL GENETICS, 1998, 35 (02) : 151 - 152
  • [50] Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population
    El Fizazi, Khawla
    Abbassi, Meriame
    Nmer, Samira
    Laamarti, Hajar
    Elalami, Mohamed Noureddine
    Ouldim, Karim
    Bouguenouch, Laila
    Ridal, Mohammed
    [J]. AUDIOLOGY AND NEUROTOLOGY, 2024, 29 (03) : 216 - 223
12345