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- 2011
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Mark
Molecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations
(
- Contribution to journal › Article
- 1997
-
Mark
Hypocomplementemia caused by C3 nephritic factors (C3 NeF): clinical findings and the coincidence of C3 NeF type II with anti-C1q autoantibodies.
(
- Contribution to journal › Article
-
Mark
Hypocomplementaemia caused by C3 nephritic factors (C3 NeF): clinical findings and the coincidence of C3 NeF type II with anti-C1q autoantibodies
(
- Contribution to journal › Article