Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families

by Winbo, Annika, Stattin, Eva-Lena, Nordin, Charlotte, Diamant, Ulla-Britt, Persson, Johan, Jensen, Steen M, Rydberg, Annika
Published 2014

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

by Stattin, Eva-Lena, Boström, Ida Maria, Winbo, Annika, Cederquist, Kristina, Jonasson, Jenni, Jonsson, Björn-Anders, Diamant, Ulla-Britt, Jensen, Steen M, Rydberg, Annika, Norberg, Anna
Published 2012