Fig. 3From: 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 genesPedigree showing individuals with hearing loss marked with filled yellow symbols with a short lower arrow (suspected Jervell & Lange-Nielsen Syndrome). LQTS as in Fig. 1. Admixture from an outside origin is marked with filled red symbolsBack to article page