A FULLY ADAPTED HEADSTAGE WITH CUSTOM ELECTRODE ARRAYS DESIGNED FOR ELECTROPHYSIOLOGICAL EXPERIMENTS



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

Abstract Background Genealogy and molecular genetic studies of a Swedish river valley population resulted in a large pedigree, showing that the hereditary hemochromatosis (HH) HFE/p.C282Y mutation is inherited with other recessive disorders such as Wilson´s disease (WND), a rare recessive disorder of copper overload.The population also contain ind

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