| 1 | CVID2, TNFRSF13B
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| A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.
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| Lougaris V, Gallizzi R, Vitali M, Baronio M, Salpietro A, Bergbreiter A, Salzer U, Badolato R, Plebani A.
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| Hum Immunol 73(8):836-9. doi: 10.1016/j.humimm.2012.05.001. Epub 2012 May 22.
2012
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| 2 | CVID2, TNFRSF13B
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| Novel Mutations in TACI (TNFRSF13B) Causing Common Variable Immunodeficiency.
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| Mohammadi J, Liu C, Aghamohammadi A, Bergbreiter A, Du L, Lu J, Rezaei N, Amirzargar AA, Moin M, Salzer U, Pan-Hammarström Q, Hammarström L.
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| J Clin Immunol Clin Immunol. 2009 Jul 23. [Epub ahead of print]
2009
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| 3 | CVID2, TNFSF13, TNFSF13B, TNFRSF13B
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| Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.
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| Salzer U, Chapel HM, Webster AD, Pan-Hammarstrom Q, Schmitt-Graeff A, Schlesier M, Peter HH, Rockstroh JK, Schneider P, Schaffer AA, Hammarstrom L, Grimbacher B.
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| Nat Genet 37(8):820-8. Epub 2005 Jul 10. 2005
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| 4 | CVID2, TNFSF13, TNFSF13B, TNFRSF13B
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| TACI is mutant in common variable immunodeficiency and IgA deficiency.
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| Castigli E, Wilson SA, Garibyan L, Rachid R, Bonilla F, Schneider L, Geha RS.
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| Nat Genet 37(8):829-34. Epub 2005 Jul 10. 2005
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| 5 | CVID2, CVID3, CVID8
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| Tackling the heterogeneity of CVID.
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| Goldacker S, Warnatz K.
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| Curr Opin Allergy Clin Immunol 5(6):504-9. Review. 2005
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