Publication | Closed Access
High incidence of <scp>FXI</scp> deficiency in a Spanish town caused by 11 different mutations and the first duplication of <i>F11</i>: Results from the Yecla study
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Citations
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References
2017
Year
Our population-cohort study supplies new evidences that FXI deficiency in Caucasians is more common than previously thought and confirmed the wide underlying genetic heterogeneity, caused by both recurrent and sporadic mutations.
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