The homozygous variant p.Gln1311 in exon 28 of VWF is associated with the development of alloantibodies in 3 unrelated patients with type 3 VWD

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Bibliographic Details
Published in:Haemophilia : the official journal of the World Federation of Hemophilia 2021-07, Vol.27 (4), p.e491-e494
Main Authors: Lassalle, Fanny, Zawadzki, Christophe, Harroche, Annie, Biron‐Andréani, Christine, Falaise, Céline, Boisseau, Pierre, Duployez, Nicolas, Jeanpierre, Emmanuelle, Rauch, Antoine, Paris, Camille, Susen, Sophie, Goudemand, Jenny
Format: Article
Language:English
Subjects:
Adolescent
Alloantibodies
Child
Exons - genetics
Female
Genetics
Hematology
Human genetics
Human health and pathology
Humans
Isoantibodies
Life Sciences
Male
von Willebrand Disease, Type 3
von Willebrand Diseases - genetics
von Willebrand Factor - genetics
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ISSN:1351-8216
1365-2516
DOI:10.1111/hae.14207