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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

Detalles Bibliográficos
Autores principales:	Fan, Junjie, Ling, Jing, Zhou, Huifeng, He, Jie, Hu, Shaoyan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Galenos Publishing 2020
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702659/ https://www.ncbi.nlm.nih.gov/pubmed/32618441 http://dx.doi.org/10.4274/tjh.galenos.2020.2020.0213

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