Frequency and distribution of FCN2 and FCN3 functional variants among MBL2 genotypes

Author:

Bjarnadottir HelgaORCID,Arnardottir Margret,Ludviksson Bjorn Runar

Funder

The Icelandic Centre for Research

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Immunology

Reference88 articles.

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2. Bjarnadottir H, Ludviksson BR (2010) Inherited deficiency of the initiator molecules of the lectin-complement pathway. Laeknabladid 96:611–617

3. Bjarnadottir H, Thorsteinsdottir V, Jorgensen G, Arnardottir M, Ludviksson B (2014) Mannan-binding lectin (MBL) deficient individuals with the O/O genotype are highly susceptible to gastrointestinal diseases. J Clin Cell Immunol 5:182

4. Boldt AB, Grisbach C, Steffensen R, Thiel S, Kun JF, Jensenius JC, Messias-Reason IJ (2011) Multiplex sequence-specific polymerase chain reaction reveals new MASP2 haplotypes associated with MASP-2 and MAp19 serum levels. Hum Immunol 72:753–760

5. Cedzynski M, Atkinson AP, St Swierzko A, Macdonald SL, Szala A, Zeman K, Buczylko K, Bak-Romaniszyn L, Wiszniewska M, Matsushita M, Szemraj J, Banasik M, Turner ML, Kilpatrick DC (2009) L-ficolin (ficolin-2) insufficiency is associated with combined allergic and infectious respiratory disease in children. Mol Immunol 47:415–419

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