Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon

Author:

Fredrikson Gunilla Nordin,Gullstrand Birgitta,Schneider Peter M,Witzel-Schlömp Konstanze,Sjöholm Anders G,Alper Chester A,Awdeh Zuheir,Truedsson Lennart

Publisher

Elsevier BV

Subject

General Medicine,Immunology,Immunology and Allergy

Reference30 articles.

1. A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B;Carroll;Nature,1984

2. The complete exon-intron structure of a human complement component C4A gene. DNA sequences, polymorphism and linkage to the 21-hydroxylase gene;Yu;J Immunol,1991

3. Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man;Carroll;Proc Natl Acad Sci USA,1985

4. C4B gene polymorphism detected in a human cosmid clone;Prentice;Immunogenetics,1986

5. Polymorphism of the human complement C4 and steroid 21-hydroxylase genes;Schneider;J Clin Invest,1986

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