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アイテム / Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A > C substitution / [No FileName]
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公開日 | 2020-09-01 | |||||
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本文URL | https://soar-ir.repo.nii.ac.jp/?action=repository_action_common_download&item_id=3778&item_no=1&attribute_id=65&file_no=1 |
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