|?|| (G;G) (G;T) (T;T) ||28|
] 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 23423485] Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China
[PMID 22848725] Mannose-binding lectin deficiency is associated with myocardial infarction: the HUNT2 study in Norway.
[PMID 22892990] The functional polymorphism Ala258Ser in the innate receptor gene ficolin-2 in the donor predicts improved renal transplant outcome.
[PMID 22940091] Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients.
[PMID 23525825] Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.