Case Report: Laboratory detection of a thrombotic tendency in a family with hypodysfibrinogenemia and a novel FGG mutation.
Monard A, Castoldi E, De Simone I, Wichapong K, van Duijl T, van den Biggelaar M, Spada S, van Doorn W, Hellenbrand D, van der Meijden P, Swieringa F, Stork A, Ten Cate H, Beckers E, Heubel-Moenen F, Henskens Y.
Monard A, et al. Among authors: van doorn w.
Front Cardiovasc Med. 2024 Oct 15;11:1488602. doi: 10.3389/fcvm.2024.1488602. eCollection 2024.
Front Cardiovasc Med. 2024.
PMID: 39473893
Free PMC article.