Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder

por Ceznerová, Eliška, Kaufmanová, Jiřina, Sovová, Žofie, Štikarová, Jana, Loužil, Jan, Kotlín, Roman, Suttnar, Jiří
Publicado 2022

Diagnosing Czech Patients with Inherited Platelet Disorders

por Louzil, Jan, Stikarova, Jana, Provaznikova, Dana, Hrachovinova, Ingrid, Fenclova, Tereza, Musil, Jan, Radek, Martin, Kaufmanova, Jirina, Geierova, Vera, Ceznerova, Eliska, Salaj, Peter, Kotlin, Roman
Publicado 2022