The Old and the New in Prekallikrein Deficiency: Historical Context and a Family from Argentina with PK Deficiency due to a New Mutation (Arg541Gln) in Exon 14 Associated with a Common Polymorphysm (Asn124Ser) in Exon 5
Girolami, Antonio, Vidal, Josè, Salagh, Marcela, Gervan, Nora, Parody, Maria, Peroni, Edoardo, Sambado, Luisa, Guglielmone, HugoVolume:
40
Language:
english
Journal:
Seminars in Thrombosis and Hemostasis
DOI:
10.1055/s-0034-1384767
Date:
July, 2014
File:
PDF, 221 KB
english, 2014