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, A; Vidal, J; Salagh, M (Semin Thromb Hemost, 2014)
, et al.