1. A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly. (28th May 2015) Authors: Srour, M.; Hamdan, F. F.; Gan‐Or, Z.; Labuda, D.; Nassif, C.; Oskoui, M.; Gana‐Weisz, M.; Orr‐Urtreger, A.; Rouleau, G.A.; Michaud, J.L. Journal: Clinical genetics Issue: Volume 88:Number 1(2015:Jul.) Page Start: E1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗