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Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation

Turkish journal of haematology : official journal of Turkish Society of Haematology - 19 Nov 2020

Fan Junjie, Ling Jing, Zhou Huifeng, He Jie, Hu Shaoyan

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 32618441
DOI: 10.4274/tjh.galenos.2020.2020.0213
PMCID: PMC7702659

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