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Dive into the research topics of 'De Novo L509P Mutation of the TGFBI Gene Associated with Slit-Lamp Findings of Lattice Corneal Dystrophy Type IIIA'. Together they form a unique fingerprint.- Sort by
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Yong Woo Ji, Hyunmin Ahn, Kyoung Jin Shin, Tae Im Kim, Kyoung Yul Seo, R. Doyle Stulting, Eung Kweon Kim
Research output: Contribution to journal › Article › peer-review