1. A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT. Issue 8 (1st May 2013) Authors: Kvarnung, Malin; Nilsson, Daniel; Lindstrand, Anna; Korenke, G Christoph; Chiang, Samuel C C; Blennow, Elisabeth; Bergmann, Markus; Stödberg, Tommy; Mäkitie, Outi; Anderlid, Britt-Marie; Bryceson, Yenan T; Nordenskjöld, Magnus; Nordgren, Ann Journal: Journal of medical genetics Issue: Volume 50:Issue 8(2013) Page Start: 521 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗