IDENTIFICATION OF A GENE IN AUTOSOMAL DOMINANT RECURRENT CORNEAL EROSION DYSTROPHY AND CHARACTERISATION USING A ZEBRAFISH MODEL

被引：0
|
作者：
Oliver, Verity [1 ]
Markie, David [2 ]
Crosier, Phil [3 ]
Mackey, David [4 ]
Sherwin, Trevor [1 ]
McGhee, Charles [1 ,5 ]
Vincent, Andrea [1 ,5 ]
机构：
[1] Univ Auckland, Dept Ophthalmol, New Zealand Natl Eye Ctr, Fac Med & Hlth Sci, Auckland 1, New Zealand
[2] Univ Otago, Dept Pathol, Dunedin, New Zealand
[3] Univ Auckland, Dept Mol Med & Pathol, Fac Med & Hlth Sci, Auckland 1, New Zealand
[4] Univ Western Australia, Lions Eye Inst, Ctr Ophthalmol & Visual Sci, Perth, WA 6009, Australia
[5] Auckland Dist Hlth Board, Eye Dept, Greenlane Clin Ctr, Auckland, New Zealand
来源：
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY | 2014年 / 42卷
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：
P0503
引用
收藏
页码：26 / 26
页数：1
相关论文
共 50 条
  • [21] A clinical and molecular genetic study of autosomal-dominant stromal corneal dystrophy in British population
    El-Ashry, MF
    El-Aziz, MM
    Hardcastle, AJ
    Bhattacharya, SS
    Ebenezer, ND
    OPHTHALMIC RESEARCH, 2005, 37 (06) : 310 - 317
  • [22] Autosomal dominant macular dystrophy: Evidence for a novel disease-causing gene
    O'Connor, ST
    Yang, Z
    Thirumalaichary, S
    Trallis, C
    Zhang, K
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 : U172 - U172
  • [23] Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene
    Ayyagari, R
    Griesinger, IB
    Bingham, E
    Lark, KK
    Moroi, SE
    Sieving, PA
    ARCHIVES OF OPHTHALMOLOGY, 2000, 118 (01) : 85 - 92
  • [24] Autosomal dominant Stargardt-like macular dystrophy: Identification of a new family with a mutation in the ELOVL4 gene
    Vrabec, TR
    Tantri, A
    Edwards, A
    Frost, A
    Donoso, LA
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2003, 136 (03) : 542 - 545
  • [25] Identification of the gene causing autosomal dominant molar hypodontia.
    Stockton, DW
    Das, P
    Goldenberg, M
    D'Souza, R
    Patel, PI
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A48 - A48
  • [26] IDENTIFICATION OF A NEW CAUSAL GENE FOR AUTOSOMAL DOMINANT FOCAL EPILEPSIES
    Ishida, S.
    Picard, F.
    Rudolf, G.
    Thomas, P.
    Genton, P.
    Marescaux, C.
    Baulac, M.
    Hirsch, E.
    Leguern, E.
    Baulac, S.
    EPILEPSIA, 2013, 54 : 14 - 15
  • [27] RECURRENT CORNEAL EROSION, MICROCYSTIC EPITHELIAL DYSTROPHY, MAP CONFIGURATIONS AND FINGERPRINT LINES IN THE CORNEA
    GHOSH, M
    MCCULLOCH, C
    CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE, 1986, 21 (06): : 246 - 252
  • [28] Identification of the gene responsible for the autosomal dominant form of centronuclear myopathy
    Bitoun, M
    Maugenre, S
    Jeannet, PY
    Ferrer, X
    Laforêt, P
    Fardeau, M
    Eymard, B
    Romero, N
    Guicheney, P
    NEUROMUSCULAR DISORDERS, 2005, 15 (9-10) : 716 - 716
  • [29] Identification of a novel gene for autosomal dominant and autosomal recessive long-QT syndrome
    Schulze-Bahr
    Wang, Q
    Oberti, C
    Wedekind, H
    Lange, S
    Borggrefe, M
    Towbin, JA
    Assmann, G
    Breithardt, G
    Haverkamp, W
    Funke, H
    EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 : 169 - 169
  • [30] Changes of Clinical Manifestation of Granular Corneal Deposits Because of Recurrent Corneal Erosion in Granular Corneal Dystrophy Types 1 and 2
    Han, Kyung Eun
    Chung, Woo Suk
    Kim, Terry
    Kim, Kyu Seo
    Kim, Tae-im
    Kim, Eung Kweon
    CORNEA, 2013, 32 (05) : E113 - E120
12345