Mikkola H.,1997
Mikkola H., Muszbek L., Laiho E., Syrjala M., Hamalainem E., Haramura G., Salmi T., Peltonen L., Palotie A. Molecular mechanism of a mild phenotype in coagulation factor Xlll (F Xlll) deficiency: a splicing mutation permitting partial correct splicing of F Xll A-subunit mRNA. - Blood, 1997, v. 89, p. 1279-1287.