Autosomal dominant cerebellar ataxia, deafness, and narcolepsy with amenorrhea, subclinical optic atrophy, and electroencephalographic abnormality: A case report

eNeurologicalSci. 2020 Sep 9:21:100271. doi: 10.1016/j.ensci.2020.100271. eCollection 2020 Dec.
No abstract available

Keywords: Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN); DNA methyltransferase-1; DNMT1 gene.