Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's syndrome on clinical expression (2014)
- Authors:
- Autor USP: TRAINA, FABÍOLA - FMRP
- Unidade: FMRP
- DOI: 10.1016/j.bcmd.2014.05.009
- Subjects: ANEMIA; POLIMORFISMO; NEFROPATIAS
- Language: Inglês
- Imprenta:
- Publisher place: Maryland Heights
- Date published: 2014
- Source:
- Título: Blood Cells, Molecules and Diseases
- ISSN: 1079-9796
- Volume/Número/Paginação/Ano: v. 53, n. 4, p. 246-252, 2014
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SANTOS, Andrey dos et al. Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's syndrome on clinical expression. Blood Cells, Molecules and Diseases, v. 53, n. 4, p. 246-252, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2014.05.009. Acesso em: 29 dez. 2025. -
APA
Santos, A. dos, Dantas, L. E. C., Traina, F., Albuquerque, D. M. de, Chaim, E. A., & Saad, S. T. O. (2014). Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's syndrome on clinical expression. Blood Cells, Molecules and Diseases, 53( 4), 246-252. doi:10.1016/j.bcmd.2014.05.009 -
NLM
Santos A dos, Dantas LEC, Traina F, Albuquerque DM de, Chaim EA, Saad STO. Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's syndrome on clinical expression [Internet]. Blood Cells, Molecules and Diseases. 2014 ; 53( 4): 246-252.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1016/j.bcmd.2014.05.009 -
Vancouver
Santos A dos, Dantas LEC, Traina F, Albuquerque DM de, Chaim EA, Saad STO. Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's syndrome on clinical expression [Internet]. Blood Cells, Molecules and Diseases. 2014 ; 53( 4): 246-252.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1016/j.bcmd.2014.05.009 - FMNL1 is downregulated in myelodysplastic syndromes and is involved in megakaryocytic differentiation
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Informações sobre o DOI: 10.1016/j.bcmd.2014.05.009 (Fonte: oaDOI API)
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