Open AccessCase Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation
Author(s) -
Junjie Fan,
Ling Jing,
Hongxia Zhou,
Jie He,
Shaoyan Hu
Publication year - 2020
Publication title -
turkish journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.351
H-Index - 16
ISSN - 1300-7777
DOI - 10.4274/tjh.galenos.2020.2020.0213
Subject(s) - medicine , von willebrand disease , pediatrics , disease , mutation , von willebrand factor , platelet , genetics , gene , biology