Gu J.,1997
Gu J., Jorieux S., Lavergne J.M., Ruan C., Mazurier C., Meyer D. A patient with type 2N von Willebrand disease is heterozygous for a new mutation: Gly22Glu. Demonstration of a defective expression of the second allele by the use of monoclonal antibodies. - Blood, 1997, v. 89, p. 3263-3269.
