Funding Data Link References Status API Help
Page 1 of 1 results
Sort by: relevance publication year

A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations inPIGT

Journal Article published 1 May 2013 in Journal of Medical Genetics volume 50 issue 8 on pages 521 to 528

Authors: Malin Kvarnung, Daniel Nilsson, Anna Lindstrand, G Christoph Korenke, Samuel C C Chiang, Elisabeth Blennow, Markus Bergmann, Tommy Stödberg, Outi Mäkitie, Britt-Marie Anderlid, Yenan T Bryceson, Magnus Nordenskjöld, Ann Nordgren