MSH5 is not a genetic predisposing factor for immunoglobulin A deficiency but marks the HLA-DRB1*0102 subgroup carrying susceptibility.

[1]  E. G. de la Concha,et al.  Lack of evidence of a role of XBP1 and PRDM1 polymorphisms in Spanish patients with immunoglobulin A deficiency. , 2009, Human immunology.

[2]  E. G. de la Concha,et al.  Role of polymorphisms in the TNFRSF13B (TACI) gene in Spanish patients with immunoglobulin A deficiency. , 2009, Tissue antigens.

[3]  R. Ádány,et al.  The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency , 2009, Genes and Immunity.

[4]  C. E. Schrader,et al.  Reassessment of the Role of Mut S Homolog 5 in Ig Class Switch Recombination Shows Lack of Involvement in cis- and trans-Switching1 , 2008, The Journal of Immunology.

[5]  E. G. de la Concha,et al.  Interleukin-6 gene variation in Spanish patients with immunoglobulin-A deficiency. , 2008, Human immunology.

[6]  D. Altshuler,et al.  Role for Msh5 in the regulation of Ig class switch recombination , 2007, Proceedings of the National Academy of Sciences.

[7]  R. Geha,et al.  Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency , 2007, Nature Genetics.

[8]  C. Cunningham-Rundles,et al.  Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency , 2007, Nature Genetics.

[9]  R. Geha,et al.  TACI mutation in common variable immunodeficiency and IgA deficiency , 2006, Current allergy and asthma reports.

[10]  E. G. de la Concha,et al.  Interleukin-10 polymorphisms in Spanish IgA deficiency patients: a case-control and family study , 2006, BMC Medical Genetics.

[11]  E. G. de la Concha,et al.  A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population , 2006, BMC Medical Genetics.

[12]  E. G. de la Concha,et al.  Major histocompatibility complex haplotypes in Spanish immunoglobulin A deficiency patients: a comparative fine mapping microsatellite study. , 2004, Tissue antigens.

[13]  E. G. de la Concha,et al.  MHC Susceptibility Genes to IgA Deficiency Are Located in Different Regions on Different HLA Haplotypes1 , 2002, The Journal of Immunology.

[14]  Kunze,et al.  HLA‐A, B, Cw and DRB1, DRB3/4/5, DQB1, DPB1 Frequencies in German Immunoglobulin A‐Deficient Individuals , 2000, Scandinavian journal of immunology.

[15]  L. Hammarström,et al.  Shared HLA class II-associated genetic susceptibility and resistance, related to the HLA-DQB1 gene, in IgA deficiency and common variable immunodeficiency. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[16]  P. Gregersen,et al.  IgA Deficiency and the MHC: Assessment of Relative Risk and Microheterogeneity Within the HLA A1 B8, DR3 (8.1) Haplotype , 2009, Journal of Clinical Immunology.

[17]  M. Cooper,et al.  IgA Deficiency**This article was accepted for publication on 17 January 1997. , 1997 .