Human Complement Components C4A and C4B Genetic Diversities: Complex Genotypes and Phenotypes
Author:
Affiliation:
1. Columbus Children's Research Institute and The Ohio State University Columbus Ohio
Publisher
Wiley
Subject
General Medicine,Immunology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142735.im1308s68
Reference37 articles.
1. Inherited structural polymorphism of the fourth component of human complement.
2. Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.
3. Deficiencies of Human Complement Component C4a and C4b and Heterozygosity in Length Variants of RP-C4-CYP21-TNX (Rccx) Modules in Caucasians
4. Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B
5. Genetic Sophistication of Human Complement Components C4A and C4B and RP-C4-CYP21-TNX (RCCX) Modules in the Major Histocompatibility Complex
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3. Low copy numbers of complementC4andC4Adeficiency are risk factors for myositis, its subgroups and autoantibodies;Annals of the Rheumatic Diseases;2022-09-28
4. Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases;Frontiers in Immunology;2021-10-26
5. Genes and Pseudogenes: Complexity of the RCCX Locus and Disease;Frontiers in Endocrinology;2021-07-30
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