Familial occurrence of isolated IgA deficiency associated with antibodies to IgA. Evidence against a structural gene defect
- 1 January 1974
- journal article
- Published by Wiley in European Journal of Immunology
- Vol. 4 (1) , 57-60
- https://doi.org/10.1002/eji.1830040115
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- A New Genetic Marker of Human Immunoglobulins Determined by an Allele at the α2 LocusVox Sanguinis, 1973
- ACTIVE SUPPRESSION OF IMMUNOGLOBULIN ALLOTYPE SYNTHESISThe Journal of Experimental Medicine, 1972
- Immunoglobulins on the surface of lymphocytesJournal of Clinical Investigation, 1971
- ISOLATED ABSENCE OF IgA WITH AUTOSOMAL DOMINANT INHERITANCEThe Lancet, 1971
- Familial selective deficiency of IgAThe Journal of Pediatrics, 1971
- Uncommon Gm Gene ComplexesVox Sanguinis, 1970
- Genetic markers of immunoglobulins in Japanese families Inheritance of associated markers belonging to one IgA and three IgG subclassesAnnals of Human Genetics, 1970
- FURTHER STUDIES ON THE γG-HEAVY CHAIN GENE COMPLEXES, WITH PARTICULAR REFERENCE TO THE GENETIC MARKERS Gm(g) AND Gm(n)The Journal of Experimental Medicine, 1968
- Selective gamma-A-globulin deficiency, with dominant autosomal inheritance in a Swiss family.Archives of Disease in Childhood, 1968
- Effect of Maternal Isoantibodies on the Quantitative Expression of two Allelic Genes Controlling γ-Globulin Allotypic SpecificitiesNature, 1962