Source: Movement disorders clinical practice. Unidade: FM
Subjects: EPILEPSIA, ATAXIA, MUTAÇÃO GENÉTICA
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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: 17 out. 2024. , 2018APA
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/mdc3.12610NLM
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 2024 out. 17 ] Available from: https://doi.org/10.1002/mdc3.12610Vancouver
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 2024 out. 17 ] Available from: https://doi.org/10.1002/mdc3.12610