Identification of a novel locus for non-syndromic autosomal dominant hearing loss.

被引:0
|
作者
Li, XC
Angeli, S
Friedman, TB
Friedman, RA
机构
[1] House Ear Inst, CMB, Los Angeles, CA USA
[2] Hosp San Juan de Dios, Fdn Venezolana Otol, Dept Otorhinolaryngol, Caracas, Venezuela
[3] NIDCD, LMG, NIH, Rockville, MD USA
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
1453
引用
收藏
页码:A260 / A260
页数:1
相关论文
共 50 条
  • [41] A new locus for non-syndromic autosomal dominant congenital cataract on chromosome 19.
    Kumar, V
    Singh, D
    Hennies, HC
    Sperling, K
    Singh, JR
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 477 - 477
  • [42] Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families
    Shafique, Sobia
    Siddiqi, Saima
    Schraders, Margit
    Oostrik, Jaap
    Ayub, Humaira
    Bilal, Ammad
    Ajmal, Muhammad
    Seco, Celia Zazo
    Strom, Tim M.
    Mansoor, Atika
    Mazhar, Kehkashan
    Shah, Syed Tahir A.
    Hussain, Alamdar
    Azam, Maleeha
    Kremer, Hannie
    Qamar, Raheel
    PLOS ONE, 2014, 9 (06):
  • [43] Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
    Kristien Verhoeven
    Lut Van Laer
    Karin Kirschhofer
    P. Kevin Legan
    David C. Hughes
    Isabelle Schatteman
    Margriet Verstreken
    Peter Van Hauwe
    Paul Coucke
    Achih Chen
    Richard J.H. Smith
    Thomas Somers
    F. Erwin Offeciers
    Paul Van de Heyning
    Guy P. Richardson
    Franz Wachtler
    William J. Kimberling
    Patrick J. Willems
    Paul J. Govaerts
    Guy Van Camp
    Nature Genetics, 1998, 19 : 60 - 62
  • [44] Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran
    Haghighat-Nia, Asieh
    Keiyani, Azadeh
    Nadeali, Zakiye
    Fazel-Najafabadi, Esmat
    Hosseinzadeh, Majid
    Salehi, Mansoor
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2015, 79 (11) : 1892 - 1895
  • [45] A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
    Samuel Mawuli Adadey
    Elvis Twumasi Aboagye
    Kevin Esoh
    Anushree Acharya
    Thashi Bharadwaj
    Nicole S. Lin
    Lucas Amenga-Etego
    Gordon A. Awandare
    Isabelle Schrauwen
    Suzanne M. Leal
    Ambroise Wonkam
    BMC Medical Genomics, 15
  • [46] Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss
    Lee, Kwanghyuk
    Ansar, Muhammad
    Andrade, Paula B.
    Khan, Bushra
    Santos-Cortez, Regie Lyn P.
    Ahmad, Wasim
    Leal, Suzanne M.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (02) : 315 - 321
  • [48] Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families
    Chaleshtori, M. Hashemzadeh
    Simpson, M. A.
    Farrokhi, E.
    Dolati, M.
    Rad, L. Hoghooghi
    Geshnigani, S. Amani
    Crosby, A. H.
    CLINICAL GENETICS, 2007, 72 (03) : 261 - 263
  • [49] A novel frameshift mutation in KCNQ4 in a family with autosomal recessive non-syndromic hearing loss
    Wasano, Koichiro
    Mutai, Hideki
    Obuchi, Chie
    Masuda, Sawako
    Matsunaga, Tatsuo
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2015, 463 (04) : 582 - 586
  • [50] A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
    Adadey, Samuel Mawuli
    Aboagye, Elvis Twumasi
    Esoh, Kevin
    Acharya, Anushree
    Bharadwaj, Thashi
    Lin, Nicole S.
    Amenga-Etego, Lucas
    Awandare, Gordon A.
    Schrauwen, Isabelle
    Leal, Suzanne M.
    Wonkam, Ambroise
    BMC MEDICAL GENOMICS, 2022, 15 (01)