Three deafnesses, two mouse models, one gene, TMC1

被引:0
|
作者
Gilgenkrantz, S
机构
来源
M S-MEDECINE SCIENCES | 2002年 / 18卷 / 8-9期
关键词
D O I
10.1051/medsci/20021889804
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
引用
收藏
页码:804 / 805
页数:2
相关论文
共 50 条
  • [31] High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects
    Ben Said, Mariem
    Hmani-Aifa, Mounira
    Amar, Imen
    Baig, Shahid Mahmood
    Mustapha, Mirna
    Delmaghani, Sedigheh
    Tlili, Abdelaziz
    Ghorbel, Abdelmonem
    Ayadi, Hammadi
    Van Camp, Guy
    Smith, Richard J. H.
    Tekin, Mustafa
    Masmoudi, Saber
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2010, 14 (03) : 307 - 311
  • [32] A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect
    Davoudi-Dehaghani, Elham
    Zeinali, Sirous
    Mahdieh, Nejat
    Shirkavand, Atefeh
    Bagherian, Hamideh
    Tabatabaiefar, Mohammad Amin
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2013, 77 (05) : 821 - 826
  • [33] Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families
    Xu, Pengcheng
    Xu, Jun
    Peng, Hu
    Yang, Tao
    NEURAL PLASTICITY, 2020, 2020
  • [34] One, two, three ... models for trichome patterning in Arabidopsis?
    Pesch, Marina
    Huelskamp, Martin
    CURRENT OPINION IN PLANT BIOLOGY, 2009, 12 (05) : 587 - 592
  • [35] Gene models of schizophrenia: DISC1 mouse models
    Jaaro-Peled, Hanna
    GENETIC MODELS OF SCHIZOPHRENIA, 2009, 179 : 75 - 86
  • [36] Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11
    Hilgert, N.
    Alasti, F.
    Dieltjens, N.
    Pawlik, B.
    Wollnik, B.
    Uyguner, O.
    Delmaghani, S.
    Weil, D.
    Petit, C.
    Danis, E.
    Yang, T.
    Pandelia, E.
    Petersen, M. B.
    Goossens, D.
    Favero, J. D.
    Sanati, M. H.
    Smith, R. J. H.
    Van Camp, G.
    CLINICAL GENETICS, 2008, 74 (03) : 223 - 232
  • [37] ZERO, ONE AND TWO-SWITCH MODELS OF GENE REGULATION
    Intep, Somkid
    Higham, Desmond J.
    DISCRETE AND CONTINUOUS DYNAMICAL SYSTEMS-SERIES B, 2010, 14 (02): : 495 - 513
  • [38] Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred
    Sadeghian, Ladan
    Tabatabaiefar, Mohammad Amin
    Fattahi, Najmeh
    Pourreza, Mohammad Reza
    Tahmasebi, Parisa
    Alavi, Zahra
    Chaleshtori, Morteza Hashemzadeh
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2019, 124 : 99 - 105
  • [39] Common founder effects of hereditary hemochromatosis, Wilson's disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes
    Olsson, K. Sigvard
    Walinder, Olof
    Jansson, Ulf
    Wilbe, Maria
    Bondeson, Marie-Louise
    Stattin, Eva-Lena
    Raha-Chowdhury, Ruma
    Williams, Roger
    HEREDITAS, 2017, 154 : 16
  • [40] Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes
    K. Sigvard Olsson
    Olof Wålinder
    Ulf Jansson
    Maria Wilbe
    Marie-Louise Bondeson
    Eva-Lena Stattin
    Ruma Raha-Chowdhury
    Roger Williams
    Hereditas, 154