Murray E.W.,1991

Murray E.W., Giles A.R., Lillicrap D. Recurring mutations at CpG dinucleotides and germ line mosaicism in the von Willebrand factor (vWF) gene as a cause of type IIB von Willebrand's disease (vWD). - Am.J.Hum.Genet., 1991, v. 49, p. 199.

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