Enayat M.S.,2000
Enayat M.S., Guilliiatt A.M., Surdhar G.K., Theophilus B.D.M., Hill F.G.H. A new candidate missense mutation (leu 1657 ile) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family. - Thromb.Haemost., 2000, v. 84, p. 369-3713
