Leiden University Scholarly Publications

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Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections
Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections
Novel genetic association of the VTCN1 region with rheumatoid arthritis
The major risk alleles of age-related macular degeneration (AMD) in CFH do not play a major role in rheumatoid arthritis (RA)
Complement activation by (auto-) antibodies
Genetic variants of C1q are a risk for rheumatoid arthritis