Angiotensin-converting enzyme insertion/deletion gene polymorphism is associated with dermatomyositis (2015)
- Authors:
- USP affiliated authors: SHINJO, SUELI MIEKO OBA - FM ; SHINJO, SAMUEL KATSUYUKI - FM ; MARIE, SUELY KAZUE NAGAHASHI - FM
- Unidade: FM
- DOI: 10.1177/1470320314524995
- Subjects: POLIMORFISMO; GENES; COMORBIDADE; ANGIOTENSINA II; ANGIOTENSINAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of the renin-angiotensin-aldosterone system
- ISSN: 1470-3203
- Volume/Número/Paginação/Ano: v. 16, n. 3, p. 666-671, 2015
- Status:
- Artigo aberto em periódico híbrido (Hybrid Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
SHINJO, Samuel K. et al. Angiotensin-converting enzyme insertion/deletion gene polymorphism is associated with dermatomyositis. Journal of the renin-angiotensin-aldosterone system, v. 16, n. 3, p. 666-671, 2015Tradução . . Disponível em: https://doi.org/10.1177/1470320314524995. Acesso em: 07 maio 2026. -
APA
Shinjo, S. K., Uno, M., Oba-Shinjo, S. M., & Marie, S. K. N. (2015). Angiotensin-converting enzyme insertion/deletion gene polymorphism is associated with dermatomyositis. Journal of the renin-angiotensin-aldosterone system, 16( 3), 666-671. doi:10.1177/1470320314524995 -
NLM
Shinjo SK, Uno M, Oba-Shinjo SM, Marie SKN. Angiotensin-converting enzyme insertion/deletion gene polymorphism is associated with dermatomyositis [Internet]. Journal of the renin-angiotensin-aldosterone system. 2015 ; 16( 3): 666-671.[citado 2026 maio 07 ] Available from: https://doi.org/10.1177/1470320314524995 -
Vancouver
Shinjo SK, Uno M, Oba-Shinjo SM, Marie SKN. Angiotensin-converting enzyme insertion/deletion gene polymorphism is associated with dermatomyositis [Internet]. Journal of the renin-angiotensin-aldosterone system. 2015 ; 16( 3): 666-671.[citado 2026 maio 07 ] Available from: https://doi.org/10.1177/1470320314524995 - A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation
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