Genetic influence on serum levels of lipids and apoproteins in individuals with and without coronary artery disease (1998)
- Authors:
- USP affiliated authors: ZAGO, MARCO ANTONIO - FMRP ; MARIN NETO, JOSE ANTONIO - FMRP ; SANTOS, JOSE ERNESTO DOS - FMRP
- Unidade: FMRP
- Subjects: HEMATOLOGIA; GENÉTICA MÉDICA; DOENÇAS CARDIOVASCULARES (EPIDEMIOLOGIA)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Clinical Chemistry
- Volume/Número/Paginação/Ano: v. 44, n. 6 supl. part. 2, p. A74 res. 320, 1998
- Conference titles: AACC Annual Meeting
-
ABNT
SCARTEZINI, M et al. Genetic influence on serum levels of lipids and apoproteins in individuals with and without coronary artery disease. Clinical Chemistry. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 set. 2024. , 1998 -
APA
Scartezini, M., Hotta, J. K. S., Zago, M. A., Pazin Filho, A., Marin-Neto, J. A., Santos, J. E. dos, & Assis, M. G. E. (1998). Genetic influence on serum levels of lipids and apoproteins in individuals with and without coronary artery disease. Clinical Chemistry. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Scartezini M, Hotta JKS, Zago MA, Pazin Filho A, Marin-Neto JA, Santos JE dos, Assis MGE. Genetic influence on serum levels of lipids and apoproteins in individuals with and without coronary artery disease. Clinical Chemistry. 1998 ; 44( 6 supl. part. 2): A74 res. 320.[citado 2024 set. 26 ] -
Vancouver
Scartezini M, Hotta JKS, Zago MA, Pazin Filho A, Marin-Neto JA, Santos JE dos, Assis MGE. Genetic influence on serum levels of lipids and apoproteins in individuals with and without coronary artery disease. Clinical Chemistry. 1998 ; 44( 6 supl. part. 2): A74 res. 320.[citado 2024 set. 26 ] - Familial hypercholesterolemia in Brazil
- The X-X-/E+E+ genotype of the Xbal/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample
- Genetica molecular
- The lebanese mutation as an important cause of familial hypercholesterolemia in Brazil
- Molecular basis of familial hypercholesteroleia (fh) in brazil
- Alteracoes do gene do receptor de ldl na hipercolesterolencia familiar
- High frequency of the lebanese allele of the ldlr gene among brazilian patients with familial hypercholesterolemia
- Identificacao da causa mais frequente da hipercolesterolemia familiar no brasil: mutacao ca no exon 14 do gene de receptores ldl
- Quanto estamos longe da dieta ideal?: análise da dieta habitual de coronariopatas sintomáticos
- HLA-H CYS282TYR mutation in patients with premature coronary atherosclerotic disease
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