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Post–Cardiopulmonary Bypass Coagulopathy in a Neonate With a Family History of von Willebrand Disease

✍ Scribed by Sana Ullah; Michael L. Schmitz; Kimo C. Stine; Charles E. Johnson; Sherry C. Faulkner; Jonathan J. Drummond-Webb


Book ID
117819716
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
74 KB
Volume
20
Category
Article
ISSN
1532-8422

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Type 2A is a qualitative variant of von Willebrand disease (vWD) characterized by a reduced platelet-dependent function, associated with an absence of large multimers. A G5135A transition, resulting in a glycine to arginine substitution at the codon 1629 of the von Willebrand factor, was identified