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. 2014 Nov 7;178(3):470–482. doi: 10.1111/cei.12427

Fig. 1.

Fig. 1

Pedigree of the family. Filled squares indicate male relatives harbouring the XIAP G466X mutation; shown in black are those with clear clinical symptoms and shown in grey those without. Circles with black centres indicate female carriers. Diagonal bars indicate deceased individuals.