Dyskeratosis congenita in mice deficient in ribosomal RNA modification (2003)
- Authors:
- Autor USP: REGO, EDUARDO MAGALHAES - FMRP
- Unidade: FMRP
- Assunto: DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2003
- Source:
-
ABNT
RUGGERO, Davide et al. Dyskeratosis congenita in mice deficient in ribosomal RNA modification. Science, v. 299, p. 259-262, 2003Tradução . . Acesso em: 11 jan. 2026. -
APA
Ruggero, D., Grisendi, S., Piazza, F., Rego, E. M., Mari, F., Rao, P. H., et al. (2003). Dyskeratosis congenita in mice deficient in ribosomal RNA modification. Science, 299, 259-262. -
NLM
Ruggero D, Grisendi S, Piazza F, Rego EM, Mari F, Rao PH, Cordon Cardo C, Pandolfi PP. Dyskeratosis congenita in mice deficient in ribosomal RNA modification. Science. 2003 ; 299 259-262.[citado 2026 jan. 11 ] -
Vancouver
Ruggero D, Grisendi S, Piazza F, Rego EM, Mari F, Rao PH, Cordon Cardo C, Pandolfi PP. Dyskeratosis congenita in mice deficient in ribosomal RNA modification. Science. 2003 ; 299 259-262.[citado 2026 jan. 11 ] - Florence: a randomized, double-blind, phase III pivotal study of febuxostat versus allopurinol for the prevention of tumor lysis syndrome (TLS) in patients with hematologic malignancies at intermediate to high TLS risk
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