Human C4 polymorphism: Pedigree analysis of qualitative, quantiative, and functional parameters as a basis for phenotype interpretations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00291561.pdf
Reference50 articles.
1. Alper CA (1976) Inherited structural polymorphism in human C2: Evidence for genetic linkage between C2 and Bf. J Exp Med 144: 1111?1115
2. Alper CA, Awdeh ZL, Raum DD, Yunis EJ (1983) Hypothesis: Extended major histocompatibility complex haplotypes in man: Role of alleles analogous to murine t mutants. Clin Immunol Immunopathol 24:276?285
3. Alper CA, Raum D, Karp S, Awdeh ZL, Yunis EJ (1983) Serum complement ?supergenes? of the major histocompatibility complex in man (complotypes). Vox Sang 45:62?67
4. Awdeh ZL, Alper CA (1980a) Inherited polymorphism of human C4 as revealed by desialization. Immunobiology 158:35?41
5. Awdeh ZL, Alper CA (1980b) Inherited structural polymorphism of the fourth component of human complement (C4). Proc Natl Acad Sci USA 77:3576?3580
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1. Reference Typing Report for Complement Component C4;Experimental and Clinical Immunogenetics;1998
2. Allotypes of the fourth component of complement in Korean;Japanese journal of human genetics;1992-12
3. Influence of C4 null alleles on C4 activation in systemic lupus erythematosus.;Annals of the Rheumatic Diseases;1991-04-01
4. Bullous pemphigoid in a patient with a C4 deficiency;British Journal of Dermatology;1991-03
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