Figure 2From: The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case reportSequence analysis of the C1qB gene.āA homozygous mutation was identified at the consensus splicing donor site in intron 2ā3 caused by a G-to-T transversion (c.187ā+ā1Gā>āT).Back to article page