HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing (2010)
- Authors:
- Santos, Paulo Caleb Junior de Lima
- Pereira, Alexandre C
- Cançado, Rodolfo Delfini - Irmandade da Santa Casa de Misericórdia de São Paulo (ISCMSP)
- Schttert, Isolmar T
- Sobreira, Tiago J. Paschoal
- Oliveira, Paulo S. L
- Hirata, Rosario Dominguez Crespo
- Hirata, Mario Hiroyuki
- Figueiredo, Maria Stella - Universidade Federal de São Paulo (UNIFESP)
- Chiattone, Carlos Sérgio - Irmandade da Santa Casa de Misericórdia de São Paulo (ISCMSP)
- Krieger, José Eduardo
- Guerra-Shinohara, Elvira Maria
- USP affiliated authors: HIRATA, ROSARIO DOMINGUEZ CRESPO - FCF ; HIRATA, MARIO HIROYUKI - FCF ; KRIEGER, JOSE EDUARDO - FM ; SHINOHARA, ELVIRA MARIA GUERRA - FCF
- Unidades: FCF; FM
- DOI: 10.1016/j.bcmd.2010.08.008
- Subjects: MUTAÇÃO GENÉTICA; HEMOCROMATOSE; MODELAGEM MOLECULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Blood Cells, Molecules, and Diseases
- ISSN: 1079-9796
- Volume/Número/Paginação/Ano: v. 45, n. 4, p. 302-307, 2010
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SANTOS, Paulo Caleb Junior de Lima et al. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing. Blood Cells, Molecules, and Diseases, v. 45, n. 4, p. 302-307, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2010.08.008. Acesso em: 28 mar. 2024. -
APA
Santos, P. C. J. de L., Pereira, A. C., Cançado, R. D., Schttert, I. T., Sobreira, T. J. P., Oliveira, P. S. L., et al. (2010). HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing. Blood Cells, Molecules, and Diseases, 45( 4), 302-307. doi:10.1016/j.bcmd.2010.08.008 -
NLM
Santos PCJ de L, Pereira AC, Cançado RD, Schttert IT, Sobreira TJP, Oliveira PSL, Hirata RDC, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing [Internet]. Blood Cells, Molecules, and Diseases. 2010 ; 45( 4): 302-307.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.bcmd.2010.08.008 -
Vancouver
Santos PCJ de L, Pereira AC, Cançado RD, Schttert IT, Sobreira TJP, Oliveira PSL, Hirata RDC, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing [Internet]. Blood Cells, Molecules, and Diseases. 2010 ; 45( 4): 302-307.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.bcmd.2010.08.008 - Hereditary hemochromatosis: HFE gene sequencing in brazilian patients with primary iron overload
- HFE gene sequencing in Brazilian patients with primary iron overload
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- HFE, hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload
- Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload
- Hereditary hemochromatosis: HFE gene sequencing in Brazilian patients with primary iron overload
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- Influência do polimorfismo C775G no gene da transcobalamina II (TC2) no metabolismo da cobalamina em gestantes
- The methionine synthase (MS) A2756G polymorphism is a genetic determinant of S-adenpsylmethionine (SAM) concentrations in pregnant women
- Evaluation of nutritional and genetic determinants of total homocysteine, methylmalonic acid and S-adenosylmethionine/S-adenosylhomocysteine values in Brazilian childbearing-age women
Informações sobre o DOI: 10.1016/j.bcmd.2010.08.008 (Fonte: oaDOI API)
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