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
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A. Girolami | L. Sambado | E. Peroni | H. Guglielmone | J. Vidal | Nora Gervan | Marcela Salagh | Maria Parody