The Old and the New in Prekallikrein Deficiency: Historical...

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, Hugo
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Volume:
40
Language:
english
Journal:
Seminars in Thrombosis and Hemostasis
DOI:
10.1055/s-0034-1384767
Date:
July, 2014
File:
PDF, 221 KB
english, 2014
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