Associated Papers
Genetic modifiers of long-term survival in sickle cell anemia.
Wonkam A et al.
Clinical and Translational Medicine, 2020
32898326 (PubMed )
Supplement: CTM2-10-e152-s001.pdf
Factor 11 single-nucleotide variants in women with heavy menstrual bleeding.
Wiewel-Verschueren S et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology, 2017
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.
Carmi S et al.
Nature Communications, 2014
25203624 (PubMed )
Supplement: ncomms5835-s5.xlsx › List_of_all_discovered_variants
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
Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis tools.
Saunders RE et al.
Human Mutation, 2005
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients.
Zadra G et al.
Haematologica, 2004
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