Garagiola, I., Seregni, S., Mortarino, M., Mancuso, M. E., Fasulo, M. R., Notarangelo, L. D., & Peyvandi, F. (2015). A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: Evidence for a founder effect. Mol Genet Genomic Med.

Garagiola, Isabella, Sabrina Seregni, Mimosa Mortarino, Maria Elisa Mancuso, Maria Rosaria Fasulo, Lucia Dora Notarangelo, et Flora Peyvandi. "A Recurrent F8 Mutation (c.6046C>T) Causing Hemophilia A in 8% of Northern Italian Patients: Evidence for a Founder Effect." Mol Genet Genomic Med 2015.

Garagiola, Isabella, et al. "A Recurrent F8 Mutation (c.6046C>T) Causing Hemophilia A in 8% of Northern Italian Patients: Evidence for a Founder Effect." Mol Genet Genomic Med 2015.