Source: Epilepsy Research. Unidades: IB, FM
Subjects: SÍNDROME DE ANGELMAN, EPILEPSIA, DELEÇÃO DE GENES, GENÉTICA MÉDICA
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VALENTE, Kette D et al. Angelman syndrome caused by deletion: a genotype—phenotype correlation determined by breakpoint. Epilepsy Research, v. 105, n. 1, p. 234-239, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.eplepsyres.2012.12.005. Acesso em: 01 maio 2024.APA
Valente, K. D., Varela, M. C., Koiffmann, C. P., Andrade, J. Q., Grossmann, R., Kok, F., & Marques-Dias, M. J. (2013). Angelman syndrome caused by deletion: a genotype—phenotype correlation determined by breakpoint. Epilepsy Research, 105( 1), 234-239. doi:10.1016/j.eplepsyres.2012.12.005NLM
Valente KD, Varela MC, Koiffmann CP, Andrade JQ, Grossmann R, Kok F, Marques-Dias MJ. Angelman syndrome caused by deletion: a genotype—phenotype correlation determined by breakpoint [Internet]. Epilepsy Research. 2013 ; 105( 1): 234-239.[citado 2024 maio 01 ] Available from: https://doi.org/10.1016/j.eplepsyres.2012.12.005Vancouver
Valente KD, Varela MC, Koiffmann CP, Andrade JQ, Grossmann R, Kok F, Marques-Dias MJ. Angelman syndrome caused by deletion: a genotype—phenotype correlation determined by breakpoint [Internet]. Epilepsy Research. 2013 ; 105( 1): 234-239.[citado 2024 maio 01 ] Available from: https://doi.org/10.1016/j.eplepsyres.2012.12.005