Godeiro Junior, Clécio de OliveiraVale, Thiago CardosoAfonso, Cintia Oliveira de MeloKok, FernandoPedroso, José LuizBarsottini, Orlando Graziani2023-06-292023-06-292018-03-13GODEIRO JUNIOR, Clécio de Oliveira; VALE, Thiago Cardoso; AFONSO, Cintia Oliveira de Melo; KOK, Fernando; PEDROSO, José Luiz; BARSOTTINI, Orlando G.. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: a novel mutation with prominent ataxia. Movement Disorders Clinical Practice, [S.L.], v. 5, n. 3, p. 330-332, 30 mar. 2018. Wiley. http://dx.doi.org/10.1002/mdc3.12610. Disponível em: https://movementdisorders.onlinelibrary.wiley.com/doi/10.1002/mdc3.12610. Acesso em: 29 jun. 2023.https://repositorio.ufrn.br/handle/123456789/52933ataxiamyoclonusepilepsyprogressive myoclonic epilepsyProgressive myoclonic epilepsy type 8 due to CERS1 deficiency: a novel mutation with prominent ataxiaarticlehttps://doi.org/10.1002/mdc3.12610