New Variant of MELAS Syndrome with Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; P.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2

by Dominique Endres, Patrick Süß, Simon Maier, Evelyn Friedel, Kathrin Alexandra Nickel, Christiane Ziegler, Bernd L. Fiebich, Franz Xaver Glocker, Friedrich Stock, Karl Egger, Thomas Lange, Michael Dacko, Nils Venhoff, Daniel Erny, Soroush Doostkam, Katalin Komlosi, Katharina Domschke, Ludger Tebartz van Elst · 2019