Fonte: Atherosclerosis. Nome do evento: Congress of the European Atherosclerosis Society. Unidades: FCF, FM
Assuntos: HIPERCOLESTEROLEMIA, MUTAÇÃO GENÉTICA, BIOQUÍMICA
ABNT
SALAZAR, Luís Antônio et al. Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2002APA
Salazar, L. A., Hirata, M. H., Cavalli, S. A., Nakandakare, E. R., Forti, N. A., Diament, J., et al. (2002). Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.NLM
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini S, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. 2002 ; 3/2 200 res. 621.[citado 2024 nov. 01 ]Vancouver
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini S, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. 2002 ; 3/2 200 res. 621.[citado 2024 nov. 01 ]