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Garagiola, I. et al. (2016). A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect. Molecular genetics & genomic medicine. 4 (2), pp. 152-159. [Online].
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Garagiola, I. et al. (2016). A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect. Molecular genetics & genomic medicine. 4 (2), pp. 152-159. [Online].