Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia (2018)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1002/mdc3.12610
- Subjects: EPILEPSIA; ATAXIA; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Movement disorders clinical practice
- ISSN: 2330-1619
- Volume/Número/Paginação/Ano: v. 5, n. 3, p. 330-332, 2018
- Status:
- Artigo possui acesso gratuito no site do editor (Bronze Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
GODEIRO JUNIOR, Clecio de Oliveira et al. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia. Movement disorders clinical practice. Hoboken: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/mdc3.12610. Acesso em: 07 maio 2026. , 2018 -
APA
Godeiro Junior, C. de O., Kok, F., Vale, T. C., Afonso, C. O. de M., Pedroso, J. L., & Barsotiini, O. G. (2018). Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia. Movement disorders clinical practice. Hoboken: Faculdade de Medicina, Universidade de São Paulo. doi:10.1002/mdc3.12610 -
NLM
Godeiro Junior C de O, Kok F, Vale TC, Afonso CO de M, Pedroso JL, Barsotiini OG. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia [Internet]. Movement disorders clinical practice. 2018 ; 5( 3): 330-332.[citado 2026 maio 07 ] Available from: https://doi.org/10.1002/mdc3.12610 -
Vancouver
Godeiro Junior C de O, Kok F, Vale TC, Afonso CO de M, Pedroso JL, Barsotiini OG. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia [Internet]. Movement disorders clinical practice. 2018 ; 5( 3): 330-332.[citado 2026 maio 07 ] Available from: https://doi.org/10.1002/mdc3.12610 - Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP
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