A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

Case 1. How interesting - so close. It was absolutely correct from the history to focus on optic atrophy and intellectual disability with very variable movement disorders https://t.co/xZLi5eVU5i #MDSCongress

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability: M... http://t.co/tYnO3viEGH