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Dive into the research topics of 'A family with hereditary factor X deficiency with a point mutation Gla32 to Gln in the Gla domain (factor X Tokyo)'. Together they form a unique fingerprint.- Sort by
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Takeru Zama, Mitsuru Murata, Reiko Watanabe, Kenji Yokoyama, Takanori Moriki, Hironobu Ambo, Hiroshi Murakami, Masao Kikuchi, Yasuo Ikeda
Research output: Contribution to journal › Article › peer-review