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APA Citation
Kvarnung, M., Nilsson, D., Lindstrand, A., Korenke, G. C., Chiang, S. C. C., Blennow, E., Bergmann, M., Stödberg, T., Mäkitie, O., Anderlid, B., Bryceson, Y. T., Nordenskjöld, M., & Nordgren, A. (2013). a novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT. Journal of medical genetics, 50(8), 521–528. http://access.bl.uk/ark:/81055/vdc_100135175786.0x000044