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. Author manuscript; available in PMC: 2013 Apr 1.
Published in final edited form as: Scand J Immunol. 2012 Apr;75(4):445–448. doi: 10.1111/j.1365-3083.2012.02674.x

Figure 1. The family pedigree with the W388X mutation in the properdin gene.

Figure 1

The index-patient is marked by an arrow. Three males IV/1, IV/2 and V/1 have the mutation. A total of six females III/2, III/3, III/5, III/20, III/21 and IV/V were shown to be carriers. In subjects marked by a star the mutation was excluded. The rest of the family members did not participate in the study. The number of children and their sexes are not known in IV/9–IV/16.