Cooney K.A. ea, 1991


Cooney K.A., Nichols W.C., Bruck M.E. et al. The molecular defect in type IIB von Willebrand disease: identification of four potential missense mutation within the putative GbIb binding domain //J. Clin. Invest. - 1991. - Vol.87. - P. 1227-1233.

Смотрите также:

  • Табл. W mut