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- NP392293.RAkLS2k-dsZ8EUY7XPzhj8luZ3dKdXKFY_TM3DzUeZNBg130_assertion type Assertion NP392293.RAkLS2k-dsZ8EUY7XPzhj8luZ3dKdXKFY_TM3DzUeZNBg130_head.
- NP392293.RAkLS2k-dsZ8EUY7XPzhj8luZ3dKdXKFY_TM3DzUeZNBg130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392293.RAkLS2k-dsZ8EUY7XPzhj8luZ3dKdXKFY_TM3DzUeZNBg130_provenance.
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