] Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.
[PMID 19220833] Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.
|| not reviewed
|| Insufficiently evaluated not reviewed
[PMID 22848725] Mannose-binding lectin deficiency is associated with myocardial infarction: the HUNT2 study in Norway.
[PMID 23525825] Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.