From: The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report
Hemolytic activity
NHS
CH50 (U/ml)
125
(NHS %)
100%
Patient serumā+āC1q (U/ml)
140
112%
Patient serumā+āC1r (U/ml)
0
0%
Patient serumā+āC1s (U/ml)
Patient serumā+āactivated C1s (U/ml)