Associated Papers
Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.
Kim J et al.
Clinical Genetics, 2012
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians.
Zadra G et al.
Haematologica, 2008
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients.
Zadra G et al.
Haematologica, 2004
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency.
Bolton-Maggs PH et al.
Journal of Thrombosis and Haemostasis : Jth, 2004
Molecular genetic analysis of factor XI deficiency: identification of five novel gene alterations and the origin of type II mutation in Portuguese families.
Ventura C et al.
Thrombosis and Haemostasis, 2000
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