Restriction fragment analysis of non-deleted complement C4 null genes suggests point mutations in C4A null alleles, but gene conversions in C4B null alleles
- PMID: 2574160
- DOI: 10.1007/BF02421186
Restriction fragment analysis of non-deleted complement C4 null genes suggests point mutations in C4A null alleles, but gene conversions in C4B null alleles
Similar articles
-
Heterogeneity in the structural basis of the human complement C4A null allele (C4A Q0) as revealed by HindIII restriction fragment length polymorphism analysis.FEBS Lett. 1987 Jun 8;217(1):65-8. doi: 10.1016/0014-5793(87)81244-9. FEBS Lett. 1987. PMID: 2885219
-
DNA polymorphism of human HLA-linked complement C4 allotypes, including C4 null alleles, in the Finnish population.Hum Hered. 1987;37(4):241-9. doi: 10.1159/000153711. Hum Hered. 1987. PMID: 2888726
-
Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus.J Exp Med. 1990 Jan 1;171(1):129-40. doi: 10.1084/jem.171.1.129. J Exp Med. 1990. PMID: 2295875 Free PMC article.
-
Polymorphism of the human complement component C4.Exp Clin Immunogenet. 1990;7(1):69-84. Exp Clin Immunogenet. 1990. PMID: 1971760 Review.
-
Inherited deficiency of the fourth component of human complement.Immunodefic Rev. 1988;1(1):3-22. Immunodefic Rev. 1988. PMID: 3078708 Review.
Cited by
-
Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4.J Clin Immunol. 1997 Mar;17(2):176-84. doi: 10.1023/a:1027334716982. J Clin Immunol. 1997. PMID: 9083894
-
Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene cluster.Nucleic Acids Res. 1994 Dec 11;22(24):5211-7. doi: 10.1093/nar/22.24.5211. Nucleic Acids Res. 1994. PMID: 7816608 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Miscellaneous