A novel, homozygous mutation in GFI1B causing inherited thrombocytopenia with Glanzmann-like platelet dysfunction

Autor: C Zaninetti, K Selleng, T Thiele, J Wesche, M Rath, U Felbor, A Greinacher
Rok vydání: 2023
Zdroj: GTH Congress 2023 – 67th Annual Meeting of the Society of Thrombosis and Haemostasis Research – The patient as a benchmark.
ISSN: 2567-5761
DOI: 10.1055/s-0042-1760615
Databáze: OpenAIRE