ATP6V1B2-related epileptic encephalopathy (2020)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1684/epd.2020.1166
- Subjects: DOENÇAS CEREBRAIS; EPILEPSIA; SURDEZ
- Language: Inglês
- Imprenta:
- Source:
- Título: Epileptic disorders
- ISSN: 1294-9361
- Volume/Número/Paginação/Ano: v. 22, n. 3, p. 317-322, 2020
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
INUZUKA, Luciana Midori et al. ATP6V1B2-related epileptic encephalopathy. Epileptic disorders, v. 22, n. 3, p. 317-322, 2020Tradução . . Disponível em: https://doi.org/10.1684/epd.2020.1166. Acesso em: 05 mar. 2026. -
APA
Inuzuka, L. M., Macedo-souza, L. I., Della-Rippa, B., Monteiro, F. P., Delgado, D. de S., Godoy, L. F., et al. (2020). ATP6V1B2-related epileptic encephalopathy. Epileptic disorders, 22( 3), 317-322. doi:10.1684/epd.2020.1166 -
NLM
Inuzuka LM, Macedo-souza LI, Della-Rippa B, Monteiro FP, Delgado D de S, Godoy LF, Ramos L, Costa LS de A, Garzon E, Kok F. ATP6V1B2-related epileptic encephalopathy [Internet]. Epileptic disorders. 2020 ; 22( 3): 317-322.[citado 2026 mar. 05 ] Available from: https://doi.org/10.1684/epd.2020.1166 -
Vancouver
Inuzuka LM, Macedo-souza LI, Della-Rippa B, Monteiro FP, Delgado D de S, Godoy LF, Ramos L, Costa LS de A, Garzon E, Kok F. ATP6V1B2-related epileptic encephalopathy [Internet]. Epileptic disorders. 2020 ; 22( 3): 317-322.[citado 2026 mar. 05 ] Available from: https://doi.org/10.1684/epd.2020.1166 - Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP
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Informações sobre o DOI: 10.1684/epd.2020.1166 (Fonte: oaDOI API)
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