Article
Molecular basis of hereditary C1q deficiency.
Immunobiology - 1 Aug 1998
Petry F
Abstract excerpt
Complete selective deficiencies of the complement component C1q are rare genetic disorders which are associated with recurrent infections and a high prevalence of lupus erythematosus-like symptoms. The improvements in molecular biology techniques have facilitated the analysis of such genetic defe...
Topics
- Amino Acid Substitution
- Autoimmune Diseases
- Chromosomes, Human, Pair 1
- Codon, Nonsense
- Complement C1q
- Female
- Genetic Predisposition to Disease
- Genotype
- Germany
- Humans
- Immunologic Deficiency Syndromes
- Lupus Erythematosus, Systemic
- Male
- Point Mutation
- Saudi Arabia
- Sequence Deletion
- Turkey