Elucidation of the OTOA paralogous sequence in non-syndromic deafness

被引:0
|
作者
Tesovnik, Tine [1 ,2 ]
Podkrajsek, Katarina Trebusak [1 ,3 ]
Sket, Robert [1 ,2 ]
Debeljak, Marusa [1 ,4 ]
Battelino, Saba [5 ,6 ]
Kovac, Jernej [1 ,2 ]
Bizjan, Barbara Jenko [1 ,2 ]
机构
[1] Univ Med Ctr Ljubljana, Clin Inst Special Lab Diagnost, Ljubljana, Slovenia
[2] Univ Ljubljana, Dept Paediat, Fac Med, Ljubljana, Slovenia
[3] Univ Ljubljana, Inst Biochem, Fac Med, Ljubljana, Slovenia
[4] Univ Ljubljana, Inst Cell Biol, Fac Med, Ljubljana, Slovenia
[5] Univ Med Ctr Ljubljana, Dept Otorhinolaryngol & Cervicofacial Surg, Ljubljana, Slovenia
[6] Univ Ljubljana, Dept Otorhinolaringol, Fac Med, Ljubljana, Slovenia
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P04.023.D
引用
收藏
页码:1334 / 1335
页数:2
相关论文
共 50 条
  • [1] Hair phenotype in non-syndromic deafness
    Volo, T.
    Sathiyaseelan, T.
    Astolfi, L.
    Guaran, V.
    Trevisi, P.
    Emanuelli, E.
    Martini, A.
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2013, 77 (08) : 1280 - 1285
  • [2] ANIMAL MODELS OF NON-SYNDROMIC HEREDITARY DEAFNESS
    Ikeda, Katsuhisa
    JOURNAL OF PHYSIOLOGICAL SCIENCES, 2009, 59 : 76 - 76
  • [3] Non-syndromic autosomal-dominant deafness
    Petersen, MB
    CLINICAL GENETICS, 2002, 62 (01) : 1 - 13
  • [4] Non-syndromic, autosomal-recessive deafness
    Petersen, MB
    Willems, PJ
    CLINICAL GENETICS, 2006, 69 (05) : 371 - 392
  • [5] A mutation in PDS causes non-syndromic recessive deafness
    Li, XC
    Everett, LA
    Lalwani, AK
    Desmukh, D
    Friedman, TB
    Green, ED
    Wilcox, ER
    NATURE GENETICS, 1998, 18 (03) : 215 - 217
  • [6] A mutation in PDS causes non-syndromic recessive deafness
    Xiaoyan C. Li
    Lorraine A. Everett
    Anil K. Lalwani
    Dilip Desmukh
    Thomas B. Friedman
    Eric D. Green
    Edward R. Wilcox
    Nature Genetics, 1998, 18 : 215 - 217
  • [7] Gene Screening for Non-Syndromic Deafness in Hainanese Patients
    Fu, Yifei
    Zhao, Zhibin
    Zheng, Jing
    Zhu, Yuanping
    Sun, Liang
    JOURNAL OF INTERNATIONAL ADVANCED OTOLOGY, 2023, 19 (04): : 283 - 287
  • [8] Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss
    Bademci, G.
    Cengiz, F. B.
    Foster, J., II
    Duman, D.
    Sennaroglu, L.
    Diaz-Horta, O.
    Atik, T.
    Kirazli, T.
    Olgun, L.
    Alper, H.
    Menendez, I.
    Loclar, I.
    Sennaroglu, G.
    Tokgoz-Yilmaz, S.
    Guo, S.
    Olgun, Y.
    Mahdieh, N.
    Bonyadi, M.
    Bozan, N.
    Ayral, A.
    Ozkinay, F.
    Yildirim-Baylan, M.
    Blanton, S. H.
    Tekin, M.
    SCIENTIFIC REPORTS, 2016, 6
  • [9] Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss
    G. Bademci
    F. B. Cengiz
    J. Foster II
    D. Duman
    L. Sennaroglu
    O. Diaz-Horta
    T. Atik
    T. Kirazli
    L. Olgun
    H. Alper
    I. Menendez
    I. Loclar
    G. Sennaroglu
    S. Tokgoz-Yilmaz
    S. Guo
    Y. Olgun
    N. Mahdieh
    M. Bonyadi
    N. Bozan
    A. Ayral
    F. Ozkinay
    M. Yildirim-Baylan
    S. H. Blanton
    M. Tekin
    Scientific Reports, 6
  • [10] Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families
    Lee, K.
    Chiu, I.
    Santos-Cortez, R. L. P.
    Basit, S.
    Khan, S.
    Azeem, Z.
    Andrade, P. B.
    Kim, S. S.
    Ahmad, W.
    Leal, S. M.
    CLINICAL GENETICS, 2013, 84 (03) : 294 - 296