Source: Dementia & Neuropsychologia. Unidade: FM
Subjects: GENES, DOENÇA DE PRÍON, DOENÇAS NEURODEGENERATIVAS, TRANSTORNOS COGNITIVOS, PROTEÍNAS (ANÁLISE), BRASIL
ABNT
SMID, Jerusa et al. Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil. Dementia & Neuropsychologia, v. 1, n. 2 p. 222-224, 2007Tradução . . Disponível em: https://doi.org/10.1590/s1980-57642008dn10200017. Acesso em: 06 set. 2024.APA
Smid, J., Martins, V. R., Landemberger, M. C., Riva, D., Anghinah, R., & Nitrini, R. (2007). Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil. Dementia & Neuropsychologia, 1( 2 p. 222-224). doi:10.1590/s1980-57642008dn10200017NLM
Smid J, Martins VR, Landemberger MC, Riva D, Anghinah R, Nitrini R. Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil [Internet]. Dementia & Neuropsychologia. 2007 ; 1( 2 p. 222-224):[citado 2024 set. 06 ] Available from: https://doi.org/10.1590/s1980-57642008dn10200017Vancouver
Smid J, Martins VR, Landemberger MC, Riva D, Anghinah R, Nitrini R. Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil [Internet]. Dementia & Neuropsychologia. 2007 ; 1( 2 p. 222-224):[citado 2024 set. 06 ] Available from: https://doi.org/10.1590/s1980-57642008dn10200017