DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy (2015)
- Authors:
- USP affiliated authors: ZANOTELI, EDMAR - FM ; CHADI, GERSON - FM ; REED, UMBERTINA CONTI - FM
- Unidade: FM
- DOI: 10.1590/S1415-4757382220140238
- Subjects: ESTUDOS DE COORTES; BRASILEIROS; MIOPATIAS CONGÊNITAS ESTRUTURAIS; MUTAÇÃO GENÉTICA; DOANÇAS CONGÊNITAS
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirão Preto
- Date published: 2015
- Source:
- Título: Genetics and Molecular Biology
- ISSN: 1415-4757
- Volume/Número/Paginação/Ano: v. 38, n. 2, p. 147-151, 2015
- Este artigo possui versão em acesso aberto
- URL de acesso aberto
- PDF de acesso aberto
- Versão do Documento: Versão publicada (Published version)
-
Status: Artigo publicado em periódico de acesso aberto (Gold Open Access) -
ABNT
ABATH NETO, Osorio et al. DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy. Genetics and Molecular Biology, v. 38, n. 2, p. 147-151, 2015Tradução . . Disponível em: https://doi.org/10.1590/S1415-4757382220140238. Acesso em: 11 mar. 2026. -
APA
Abath Neto, O., Martins, C. de A., Carvalho, M., Chadi, G., Seitz, K. W., Oliveira, A. S. B., et al. (2015). DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy. Genetics and Molecular Biology, 38( 2), 147-151. doi:10.1590/S1415-4757382220140238 -
NLM
Abath Neto O, Martins C de A, Carvalho M, Chadi G, Seitz KW, Oliveira ASB, Reed UC, Laporte J, Zanoteli E. DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy [Internet]. Genetics and Molecular Biology. 2015 ; 38( 2): 147-151.[citado 2026 mar. 11 ] Available from: https://doi.org/10.1590/S1415-4757382220140238 -
Vancouver
Abath Neto O, Martins C de A, Carvalho M, Chadi G, Seitz KW, Oliveira ASB, Reed UC, Laporte J, Zanoteli E. DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy [Internet]. Genetics and Molecular Biology. 2015 ; 38( 2): 147-151.[citado 2026 mar. 11 ] Available from: https://doi.org/10.1590/S1415-4757382220140238 - Clinical aspects of patients with sarcoglycanopathies under steroids therapy
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