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Dive into the research topics of 'The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients'. Together they form a unique fingerprint.- Sort by
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Minako Konishi, Yukihiko Mashima, Masakazu Yamada, Jun Kudoh, Nobuyoshi Shimizu
Research output: Contribution to journal › Article › peer-review