Sex influences transmission of the supratype associated with the C2 deficiency allele: A possible mechanism for the maintenance of heterozygosity and disease susceptibility

This publication has 26 references indexed in Scilit:

• The Coexistence of IgA Deficiency and 21-Hydroxylase Deficiency Marked by Specific MHC Supratypes
  Annals of the New York Academy of Sciences, 1985
• Differences in Risk of Insulin-Dependent Diabetes in Offspring of Diabetic Mothers and Diabetic Fathers
  New England Journal of Medicine, 1984
• Familial discoid lupus erythematosus associated with heterozygote c2 deficiency
  Arthritis & Rheumatism, 1980
• Linkage Relationship of C2 Deficiency, HLA and Glyoxalase I Loci¹
  Vox Sanguinis, 1979
• Homozygous C2 deficiency with fulminant lupus erythematosus. severe nephritis via the alternative complement pathway
  Arthritis & Rheumatism, 1978
• The chromosomal order of genes controlling the major histocompatibility complex, properdin factor B, and deficiency of the second component of complement.
  Journal of Clinical Investigation, 1976
• HYPOCOMPLEMENTÆMIC MULTIPLE SCLEROSIS: HETEROZYGOUS C2 DEFICIENCY LINKED TO HLA A10, B18
  The Lancet, 1976
• Linkage of Gene for C2 Deficiency and the Major Histocompatibility Complex MHC in Man Family Study of a Further Case¹
  Vox Sanguinis, 1976
• Hereditary C2 deficiency: Genetic studies and association with the HL-A system.
  The Journal of Experimental Medicine, 1975
• EVIDENCE FOR LINKAGE BETWEEN HL-A HISTOCOMPATIBILITY GENES AND THOSE INVOLVED IN THE SYNTHESIS OF THE SECOND COMPONENT OF COMPLEMENT
  The Journal of Experimental Medicine, 1974