The autosomal recessive non-syndromic deafness loci, DFNB8 and DFNB10 on human chromosome 21q22.3, are distinct loci.

被引：0
|
作者：
Scott, HS
Berry, A
Korostishevsky, M
Talior, I
Barras, C
Gehrig, C
Younus, F
Veske, A
Mohyuddin, A
Mehdi, SQ
Gal, A
Kudoh, J
Shimizu, N
Bonne-Tamir, B
Antonarakis, SE
机构：
[1] Univ Geneva, Sch Med, Div Med Genet, Geneva, Switzerland
[2] Tel Aviv Univ, Sackler Sch Med, Dept Human Genet & Mol Med, IL-69978 Tel Aviv, Israel
[3] Khan Res Labs, Biomed & Genet Engn Div, Islamabad, Pakistan
[4] Univ Krankenhaus Eppendorf, Inst Humangenet, Hamburg, Germany
[5] Keio Univ, Sch Med, Dept Biol Mol, Tokyo 108, Japan
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 65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：
2523
引用
收藏
页码：A445 / A445
页数：1
相关论文
共 50 条
  • [31] DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22
    Ansar, M
    Chahrour, MH
    Din, MAU
    Arshad, M
    Haque, S
    Pham, TL
    Yan, K
    Ahmad, W
    Leal, SM
    HUMAN HEREDITY, 2004, 57 (04) : 195 - 199
  • [32] Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness
    Mirna Mustapha
    Nabiha Salem
    Dominique Weil
    Elie El-Zir
    Jacques Loiselet
    Christine Petit
    European Journal of Human Genetics, 1998, 6 : 548 - 551
  • [33] Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness
    Mustapha, M
    Salem, N
    Weil, D
    El-Zir, E
    Loiselet, J
    Petit, C
    EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 (06) : 548 - 551
  • [34] Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
    Zelante, L
    Gasparini, P
    Estivill, X
    Melchionda, S
    DAgruma, L
    Govea, N
    Mila, M
    DellaMonica, M
    Lutfi, J
    Shohat, M
    Mansfield, E
    Delgrosso, K
    Rappaport, E
    Surrey, S
    Fortina, P
    HUMAN MOLECULAR GENETICS, 1997, 6 (09) : 1605 - 1609
  • [35] A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan
    Ansar, M
    Din, MAU
    Arshad, M
    Sohail, M
    Faiyaz-Ul-Haque, M
    Haque, S
    Ahmad, W
    Leal, SM
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2003, 11 (01) : 77 - 80
  • [36] Genetic map localization of DFNA34 and DFNA36, two autosomal dominant non-syndromic deafness loci.
    Kurima, K
    Szymko, Y
    Rudy, S
    Morell, RJ
    Friedman, TB
    Griffith, AJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 300 - 300
  • [37] Connexin-26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in the Iranian Population
    Mohseni, M
    Arzhangi, S
    Cucci, RA
    Riazalhosseini, Y
    Malekpour, M
    Daneshi, A
    Farhadi, K
    Kahrizi, K
    Shafeghati, Y
    Smith, RJH
    Najmabadi, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 402 - 402
  • [38] A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1–14q24.3 in large consanguineous kindred from Pakistan
    Muhammad Ansar
    Mohammad Amin ud Din
    Muhammad Arshad
    Muhammad Sohail
    Mohammad Faiyaz-Ul-Haque
    Sayedul Haque
    Wasim Ahmad
    Suzanne M Leal
    European Journal of Human Genetics, 2003, 11 : 77 - 80
  • [39] Adult AAV Gene Therapy Rescues Auditory Function in a Mouse Model of Human TMPRSS3 Recessive Deafness DFNB8/10
    Du, Wan
    Chen, Zheng-Yi
    MOLECULAR THERAPY, 2022, 30 (04) : 571 - 571
  • [40] Autosomal recessive non-syndromic deafness(DFNA3/DFNB1): connexin 26 mutation analysis in Pakistani, Middle Eastern and Caucasian populations
    Mueller, R
    Lench, N
    Houseman, M
    Middleton, A
    Karbani, G
    Janjua, AH
    Newton, V
    Parry, G
    AlGazali, L
    Markham, AF
    JOURNAL OF MEDICAL GENETICS, 1997, 34 : SP20 - SP20
12345