Chatron, Nicolas; Becker, Felicitas; Morsy, Heba; Schmidts, Miriam; Hardies, Katia; Tuysuz, Beyhan; Roselli, Sandra; Najafi, Maryam; Alkaya, Dilek Uludag; Kok, Fernando 
Subjects: FENÓTIPOS, FISSURA PALATINA, PACIENTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHATRON, Nicolas et al. Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. Brain, v. 143, p. 1447-1461, 2020Tradução . . Disponível em: https://doi.org/10.1093/brain/awaa085. Acesso em: 27 abr. 2024.APA
Chatron, N., Becker, F., Morsy, H., Schmidts, M., Hardies, K., Tuysuz, B., et al. (2020). Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. Brain, 143, 1447-1461. doi:10.1093/brain/awaa085NLM
Chatron N, Becker F, Morsy H, Schmidts M, Hardies K, Tuysuz B, Roselli S, Najafi M, Alkaya DU, Kok F. Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy [Internet]. Brain. 2020 ; 143 1447-1461.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1093/brain/awaa085Vancouver
Chatron N, Becker F, Morsy H, Schmidts M, Hardies K, Tuysuz B, Roselli S, Najafi M, Alkaya DU, Kok F. Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy [Internet]. Brain. 2020 ; 143 1447-1461.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1093/brain/awaa085
