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Correspondences
Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
Yun Jeong Lee, Kwangsic Joo, Moon-Woo Seong, Kyu Hyung Park, Sung Sup Park, Se Joon Woo
Korean J Ophthalmol. 2020;34(2):170-172.   Published online March 16, 2020
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Retinitis Pigmentosa Associated with Bardet-Biedl Syndrome with BBS9 Gene Mutation in a Korean Patient
Yong Hoon Kim, Kwang Sic Joo, Moon-Woo Seong, Sung Sup Park, Se Joon Woo
Korean J Ophthalmol. 2020;34(1):94-95.   Published online February 4, 2020
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Bietti Crystalline Retinopathy Confirmed by Mutation of CYP4V2 Gene in a Korean Patient
Young Joo Park, Duck Jin Hwang, Moon-Woo Seong, Sung Sup Park, Se Joon Woo
Korean J Ophthalmol. 2016;30(1):81-83.   Published online January 21, 2016
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Original Articles
Brain Imaging Studies in Leber's Congenital Amaurosis: New Radiologic Findings Associated with the Complex Trait
Hee Kyung Yang, Jeong-Min Hwang, Sung Sup Park, Young Suk Yu
Korean J Ophthalmol. 2010;24(6):360-363.   Published online November 23, 2010
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Case Reports
Infantile Vitreous Hemorrhage as the Initial Presentation of X-linked Juvenile Retinoschisis
Jong Joo Lee, Jeong Hun Kim, So Yeon Kim, Sung Sup Park, Young Suk Yu
Korean J Ophthalmol. 2009;23(2):118-120.   Published online June 9, 2009
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Original Articles
Investigation of the Association between Normal-tension Glaucoma and Single Nucleotide Polymorphisms in Natriuretic Peptide Gene
Jin Wook Jeoung, Dong Myung Kim, Hyun Soo Ko et al.
Korean J Ophthalmol. 2007;21(1):33-38.   Published online March 20, 2007
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Korean Journal of
Ophthalmology

Print ISSN: 1011-8942
Online ISSN: 2092-9382



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