CYP1B1 Mutations in South Korean Patients With Primary Congenital Glaucoma : Genotype - Phenotype Correlations

被引：0
|
作者：
Suh, W. [1 ]
Kook, M. S. [2 ]
Kim, Y. Y. [3 ]
Kim, C. Y. [4 ]
Kim, C. S. [5 ]
Park, K. H. [6 ]
Park, C. K. [7 ]
Kim, H. J. [8 ]
Ki, C. S. [8 ]
Kee, C. [1 ]
机构：
[1] Sungkyunkwan Univ, Coll Med, Samsung Med Ctr, Dept Ophthalmol, Seoul, South Korea
[2] Univ Ulsan, Asan Med Ctr, Dept Ophthalmol, Seoul, South Korea
[3] Korea Univ, Coll Med, Dept Ophthalmol, Seoul, South Korea
[4] Yonsei Univ, Coll Med, Dept Ophthalmol, Seoul, South Korea
[5] Chungnam Natl Univ Hosp, Dept Ophthalmol, Daejon, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Ophthalmol, Seoul, South Korea
[7] Catholic Univ Korea, Coll Med, Dept Ophthalmol & Visual Sci, Seoul, South Korea
[8] Sungkyunkwan Univ, Coll Med, Samsung Med Ctr, Dept Lab Med & Genet, Seoul, South Korea
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2010年 / 51卷 / 13期
关键词：
gene screening; clinical (human) or epidemiologic studies: prevalence/incidence; clinical (human) or epidemiologic studies: natural history;
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
2163
引用
收藏
页数：2
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