A Sardinian founder mutation in glycoprotein Ib platelet subunit beta (GP1BB) that impacts thrombocytopenia

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	British journal of haematology 2020-12, Vol.191 (5), p.e124-e128
Hauptverfasser:	Busonero, Fabio, Steri, Maristella, Orrù, Valeria, Sole, Gabriella, Olla, Stefania, Marongiu, Michele, Maschio, Andrea, Sidore, Carlo, Lai, Sandra, Mulas, Antonella, Zoledziewska, Magdalena, Floris, Matteo, Pala, Mauro, Forabosco, Paola, Asunis, Isadora, Pitzalis, Maristella, Deidda, Francesca, Masala, Marco, Caria, Cristian Antonio, Barella, Susanna, Abecasis, Goncalo R., Schlessinger, David, Sanna, Serena, Fiorillo, Edoardo, Cucca, Francesco
Format:	Artikel
Sprache:	eng
Schlagworte:	bernard‐Soulier syndrome Female Founder Effect functional studies genetic analysis GP1BB Hematology Humans Italy Male Mutation platelet count Platelet Glycoprotein GPIb-IX Complex - genetics platelet glycoproteins Thrombocytopenia Thrombocytopenia - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!