1. Rare familial TSC2 gene mutation associated with atypical phenotype presentation of Tuberous Sclerosis Complex. Issue 3 (27th January 2017) Authors: Fox, Jonah; Ben‐Shachar, Shay; Uliel, Shimrit; Svirsky, Ran; Saitsu, Hirotomo; Matsumoto, Naomichi; Fattal‐Valevski, Aviva Journal: American journal of medical genetics Issue: Volume 173:Issue 3(2017) Page Start: 744 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗