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

Chang, Kai-ChiehKai-ChiehChangKuo, Yih-ChihYih-ChihKuoHSUEH-WEN HSUEHNI-CHUNG LEECHIH-CHAO YANGSUNG-TSANG HSIEHCHI-CHAO CHAO2020-12-102020-12-102020-1224056502https://scholars.lib.ntu.edu.tw/handle/123456789/525305enAutosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN); DNA methyltransferase-1; DNMT1 geneAutosomal dominant cerebellar ataxia, deafness, and narcolepsy with amenorrhea, subclinical optic atrophy, and electroencephalographic abnormality: A case reportletter10.1016/j.ensci.2020.10027132984563