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

Overview of attention for article published in Hereditas, December 2017

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The genetic genealogical approach with medical implications #geneticgenealogy #hemochromatosis https://t.co/Wj5yFdR0jM

RT @HfmHendrik: Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal rec... https://t…

Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal rec... https://t.co/27etQdYDfu

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