Hear come more genes!

被引:10
作者
Avraham, KB [1 ]
机构
[1] Tel Aviv Univ, Sackler Sch Med, IL-69978 Tel Aviv, Israel
关键词
D O I
10.1038/3215
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
Advances in genome research are leading to the identification of new genes for non-syndromic hearing loss.
引用
收藏
页码:1238 / 1239
页数:2
相关论文
共 5 条
  • [1] Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene
    Denoyelle, F
    Weil, D
    Maw, MA
    Wilcox, SA
    Lench, NJ
    AllenPowell, DR
    Osborn, AH
    Dahl, HHM
    Middleton, A
    Houseman, MJ
    Dode, C
    Marlin, S
    BoulilaElGgaied, A
    Grati, M
    Ayadi, H
    BenArab, S
    Bitoun, P
    LinaGranade, G
    Godet, J
    Mustapha, M
    Loiselet, J
    ElZir, E
    Aubois, A
    Joannard, A
    Levilliers, J
    Garabedian, EN
    Mueller, RF
    Gardner, RJM
    Petit, C
    [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (12) : 2173 - 2177
  • [2] GENETIC EPIDEMIOLOGY OF HEARING IMPAIRMENT
    MORTON, NE
    [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1991, 630 : 16 - 31
  • [3] ISOLATION OF NOVEL AND KNOWS GENES FROM A HUMAN FETAL COCHLEAR CDNA LIBRARY USING SUBTRACTIVE HYBRIDIZATION AND DIFFERENTIAL SCREENING
    ROBERTSON, NG
    KHETARPAL, U
    GUTIERREZESPELETA, GA
    BIEBER, FR
    MORTON, CC
    [J]. GENOMICS, 1994, 23 (01) : 42 - 50
  • [4] Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
    Robertson, NG
    Lu, L
    Heller, S
    Merchant, SN
    Eavey, RD
    McKenna, M
    Nadol, JB
    Miyamoto, RT
    Linthicum, FH
    Neto, JFL
    Hudspeth, AJ
    Seidman, CE
    Morton, CC
    Seidman, JG
    [J]. NATURE GENETICS, 1998, 20 (03) : 299 - 303
  • [5] Van Laer L, 1998, NAT GENET, V20, P194