Source: Human Mutation. Unidades: FCF, FM
Subjects: GENÉTICA, HIPERCOLESTEROLEMIA (AVALIAÇÃO), MUTAÇÃO GENÉTICA (IDENTIFICAÇÃO), TÉCNICAS E PROCEDIMENTOS DE LABORATÓRIO
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SALAZAR, Luís Antônio et al. Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations. Human Mutation, v. 19, n. 4, p. 462-463, 2002Tradução . . Disponível em: https://doi.org/10.1002/humu.9032. Acesso em: 16 ago. 2024.APA
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 seven novel LDLR gene mutations. Human Mutation, 19( 4), 462-463. doi:10.1002/humu.9032NLM
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini SD, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations [Internet]. Human Mutation. 2002 ; 19( 4): 462-463.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1002/humu.9032Vancouver
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini SD, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations [Internet]. Human Mutation. 2002 ; 19( 4): 462-463.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1002/humu.9032