Source: Resumos. Conference titles: International Symposium on Pathophysiology and Toxicology/ISPAT. Unidade: FCF
Subjects: LIPOPROTEÍNAS LDL, HIPERCOLESTEROLEMIA
ABNT
LOS, Bruna et al. Identification of the PCSK9 E32K gain-of-function mutation in a Brazilian patient with familial hypercholesterolemia: a case report. 2018, Anais.. São Paulo: FCF/USP, 2018. Disponível em: http://simpac.wixsite.com/simpac/symposium-publications. Acesso em: 16 ago. 2024.APA
Los, B., Hernandez, C. D., Borges, J. B., Bastos, G. M., Faludi, A. A., Hirata, R. D. C., & Hirata, M. H. (2018). Identification of the PCSK9 E32K gain-of-function mutation in a Brazilian patient with familial hypercholesterolemia: a case report. In Resumos. São Paulo: FCF/USP. Recuperado de http://simpac.wixsite.com/simpac/symposium-publicationsNLM
Los B, Hernandez CD, Borges JB, Bastos GM, Faludi AA, Hirata RDC, Hirata MH. Identification of the PCSK9 E32K gain-of-function mutation in a Brazilian patient with familial hypercholesterolemia: a case report [Internet]. Resumos. 2018 ;[citado 2024 ago. 16 ] Available from: http://simpac.wixsite.com/simpac/symposium-publicationsVancouver
Los B, Hernandez CD, Borges JB, Bastos GM, Faludi AA, Hirata RDC, Hirata MH. Identification of the PCSK9 E32K gain-of-function mutation in a Brazilian patient with familial hypercholesterolemia: a case report [Internet]. Resumos. 2018 ;[citado 2024 ago. 16 ] Available from: http://simpac.wixsite.com/simpac/symposium-publications