ASSESSING RHODOPSIN KINASE AS A CANDIDATE GENE FOR DOMINANT STARGARDT MACULAR DYSTROPHY

被引：0
|
作者：
ZHANG, K
SEIDMAN, CE
SEIDMAN, JG
DONOSO, LA
机构：
[1] HARVARD UNIV, SCH MED, DEPT GENET, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, HOWARD HUGHES MED INST, BOSTON, MA 02115 USA
[3] WILLS EYE HOSP & RES INST, DIV RES, PHILADELPHIA, PA 19107 USA
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 1995年 / 36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：S1064 / S1064
页数：1
相关论文
共 50 条
  • [21] Historical evolution in the understanding of Stargardt macular dystrophy
    Fishman, Gerald Allen
    OPHTHALMIC GENETICS, 2010, 31 (04) : 183 - 189
  • [22] Foveal thickness and macular volume changes in Stargardt macular dystrophy
    Hargitai, J
    Somfai, G
    Vámos, R
    Farkas, A
    Gouras, P
    Salacz, G
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 : U108 - U108
  • [23] DOMINANTLY INHERITED MACULAR DYSTROPHY WITH FLECKS (STARGARDT)
    CIBIS, GW
    MOREY, M
    HARRIS, DJ
    ARCHIVES OF OPHTHALMOLOGY, 1980, 98 (10) : 1785 - 1789
  • [24] Functional and Structural Correlations in Stargardt Macular Dystrophy
    Anastasakis, A.
    Fishman, G. A.
    Genead, M.
    Lindeman, M.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (13)
  • [25] A case of Stargardt macular dystrophy caused by uniparental isodisomy (UPID) and subsequent analysis of 830 Stargardt macular dystrophy cases for UPID
    Eliason, DA
    Affitagato, LM
    Haines, HL
    Rosenthal, EF
    Lotery, AJ
    Stone, EM
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 : U712 - U712
  • [26] The ABCR gene in recessive and dominant Stargardt diseases:: A genetic pathway in macular degeneration
    Zhang, K
    Kniazeva, M
    Hutchinson, A
    Han, M
    Dean, M
    Allikmets, R
    GENOMICS, 1999, 60 (02) : 234 - 237
  • [27] GENETIC-LINKAGE OF A STARGARDT-LIKE DOMINANT PROGRESSIVE MACULAR DYSTROPHY TO CHROMOSOME-6
    STONE, EM
    NICHOLS, BE
    KIMURA, AE
    WEINGEIST, TA
    DRACK, AV
    SHEFFIELD, VC
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1994, 35 (04) : 1717 - 1717
  • [28] Autosomal dominant stargardt macular dystrophy: Clinical features and linkage analysis in a large Greek family.
    Karan, G
    Fan, K
    Kitsos, G
    Yang, Z
    Economou-Petersen, E
    Grigoriadou, M
    Psilas, K
    Petersen, MB
    Zack, DJ
    Zhang, K
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 440 - 440
  • [29] MACULAR ATROPHY AND PHENOTYPIC VARIABILITY IN AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY DUE TO PROM1 MUTATION
    Ricca, Aaron M.
    Han, Ian C.
    Hoffmann, Jeremy
    Stone, Edwin M.
    Sohn, Elliott H.
    RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2023, 43 (07): : 1165 - 1173
  • [30] Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4
    Grayson, C
    Molday, RS
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (37) : 32521 - 32530
12345