Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Matthys, Erve" or (type any "bookEditor issueEditor" and editor="Matthys, Erve") Add to list Journal Article A1 open access Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia Nikhita Ajit Bolar, Christelle Golzio, Martina Živná, Gaëlle Hayot, CHRISTINE VAN HEMELRIJK (UGent) , Dorien Schepers, Geert Vandeweyer, Alexander Hoischen, Jeroen R Huyghe, Ann Raes (UGent) , et al. (2016) AMERICAN JOURNAL OF HUMAN GENETICS. 99(1). p.174-187