Progressive myoclonic epilepsy due to rare mitochondrial ND6 mutation, m.14487T>C
Anthony Khoo, Saadnah Naidu, Surapi Bhairavi Wijayendran, Ashirwad Merve, Fion Bremner, Meneka Kaur Sidhu
BMJ Neurology Open Jun 2021, 3 (1) e000180; DOI: 10.1136/bmjno-2021-000180