Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia
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author: Geert Mortier, Christelle Golzio, Marie-Claire Gubler, Guy Van Camp, Anna Přistoupilová, Kateřina Hodaňová, Petr Vyletal, Hana Hartmannová, Viktor Stránecký, Helena Hůlková, Veronika Barešová, Ivana Jedličková, Aleš Hnízda, Bart L Loeys, Han G. Brunner, Martina Živná, Jana Sovová, Myriam Azou, Johan Vande Walle
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