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

Internet

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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