Fig. 1From: 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 Long QT Syndrome (LQTS) and hereditary hemochromatosis (HH). LQTS are marked with half filled symbols, hemochromatosis with filled blue symbols. Double horisontal lines mark consanguineous marriagesBack to article page