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Dive into the research topics of 'A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene'. Together they form a unique fingerprint.- Sort by
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Kazuki Yasuda, Naoya Koda, Hiroko Kadowaki, Yoshihiro Ogawa, Satoshi Kimura, Takashi Kadowaki, Yasuo Akanuma
Research output: Contribution to journal › Article › peer-review