Article
Prevalence of a mutation causing C2 deficiency in systemic lupus erythematosus.
The Journal of rheumatology - 1 Jun 1994
Sullivan K E, Petri M A, Schmeckpeper B J, McLean R H, Winkelstein J A
Abstract excerpt
OBJECTIVE: In an effort to establish whether a 28 base pair (bp) deletion in the gene for the 2nd component of complement (C2) constitutes a significant genetic risk factor for systemic lupus erythematosus (SLE), we determined the frequency of this mutation in SLE and control populations. The MHC...
Topics
- Base Sequence
- Black People
- Complement C2
- Gene Deletion
- Gene Frequency
- Homozygote
- Humans
- Lupus Erythematosus, Systemic
- Major Histocompatibility Complex
- Molecular Probes
- Molecular Sequence Data
- Mutation
- Polymerase Chain Reaction
- Prevalence
- Proteins
- Reference Values
- White People
- Black or African American
