Publications by authors named "Olof Walinder"

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Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the and genes.
K Sigvard Olsson, Olof Wålinder, Ulf Jansson, Maria Wilbe, Marie-Louise Bondeson

Hereditas· April 2018

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Common local founder effects for Wilson's disease and hereditary hemochromatosis; mutation studies of a large family.
Karl Sigvard Olsson, Olof Wålinder, Andreas Kindmark, Roger Williams

Scand J Gastroenterol· September 2012

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