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 JOSE M; SABAGH M; GUGLIELMONE HUGO A

THIEME MEDICAL PUBL INC

Año: 2014 vol. 40 p. 592 - 592

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