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Fig. 6 | Hereditas

Fig. 6

From: Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes

Fig. 6

Pedigree showing the ancestry of the D 87 family with homozygosity for the TMC1/p.L605P in repeat generations. Both parents of XIII:2 share origin in a generation VIII family with hearing loss. The first HL member observed (on the 23rd of December 1715 (44) is seen as IV:16. IV:18 is the “Finnkommissioner” of the HFE family marrying into the Finnish founder family. Finnish ancestry is marked with light blue symbols

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