A new gene for dominant cone-rod dystrophy is localised to chromosome 17p

被引：0
|
作者：
Kelsell, RE
Evans, K
Gregory, CY
Moore, AT
Bird, AC
Hunt, DM
机构：
[1] UCL, INST OPHTHALMOL, DEPT MOL GENET, LONDON, ENGLAND
[2] ADDENBROOKES HOSP, DEPT OPHTHALMOL, CAMBRIDGE, ENGLAND
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 1997年 / 38卷 / 04期
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
引用
收藏
页码：3686 / 3686
页数：1
相关论文
共 50 条
  • [31] CLINICAL SUBTYPES OF CONE-ROD DYSTROPHY
    SZLYK, JP
    FISHMAN, GA
    ALEXANDER, KR
    PEACHEY, NS
    DERLACKI, DJ
    ARCHIVES OF OPHTHALMOLOGY, 1993, 111 (06) : 781 - 788
  • [32] Cone-rod dystrophy in Danon disease
    Scott Brodie
    Graefe's Archive for Clinical and Experimental Ophthalmology, 2012, 250 : 633 - 633
  • [33] Spondylometaphyseal Dysplasia With Cone-Rod Dystrophy
    Kitoh, Hiroshi
    Kaneko, Hiroshi
    Kondo, Mineo
    Yamamoto, Toshiyuki
    Ishiguro, Naoki
    Nishimura, Gen
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (04) : 845 - 849
  • [34] CONE-ROD DYSTROPHY IN GUINEA BABOON
    VAINISI, SJ
    FISHMAN, GA
    WOLF, ED
    BOESE, GK
    TRANSACTIONS AMERICAN ACADEMY OF OPHTHALMOLOGY AND OTOLARYNGOLOGY, 1976, 81 (04): : O725 - O730
  • [35] Spondylometaphyseal dysplasia with cone-rod dystrophy
    Walters, BA
    Raff, ML
    Hoeve, JV
    Tesser, R
    Leonard, LO
    France, TD
    Glass, IA
    Pauli, RM
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 129A (03) : 265 - 276
  • [36] A CRX mutation in a Finnish family with dominant cone-rod retinal dystrophy.
    Sankila, EM
    Joensuu, TH
    Hamalainsn, RH
    Raitanen, N
    Ignatius, J
    Gormand, B
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A489 - A489
  • [37] Mutation in ATP1A3 is associated with dominant cone-rod dystrophy
    Zhou, Gao-Hui
    Xiang, Lue
    Huang, Xiu-Feng
    Lei, Xin-Lan
    Lv, Ji-Neng
    Wu, Kun-Chao
    Wang, Xiao-Yun
    Jin, Zi-Bing
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2018, 59 (09)
  • [38] Abnormal cone synapses in human cone-rod dystrophy
    Gregory-Evans, K
    Fariss, RN
    Possin, DE
    Gregory-Evans, CY
    Milam, AH
    OPHTHALMOLOGY, 1998, 105 (12) : 2306 - 2312
  • [39] Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p
    Hughes, AE
    Lotery, AJ
    Silvestri, G
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (09) : 770 - 772
  • [40] A PROGRESSIVE CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA - A NEW SYNDROME
    JALILI, IK
    SMITH, NJD
    JOURNAL OF MEDICAL GENETICS, 1988, 25 (11) : 738 - 740
12345