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Clinical Features of Leber Hereditary Optic Neuropathy Carrying a Rare m.13051G>A Mitochondrial Mutation: A Case Report
Hyuna Kim, Hee Kyung Yang, Moon-Woo Seong, Jeong-Min Hwang
Korean J Ophthalmol. 2025;39(6):586-588.   Published online September 23, 2025
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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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Korean Journal of
Ophthalmology

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



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