A new NBIA patient from Turkey with homozygous C19ORF12 mutation. - Kasapkara, Çiğdem Seher; Tümer, Leyla; Gregory, Allison; Ezgü, Fatih; İnci, Aslı; Derinkuyu, Betül Emine; Fox, Rachel; Rogers, Caleb; Hayflick, Susan (Acta Neurol Belg, 2019)