Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente (2010)
- Authors:
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- Subjects: MUTAÇÃO GENÉTICA; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher place: Ospedaletto
- Date published: 2010
- Source:
- Título: Acta Myologica
- ISSN: 1128-2460
- Volume/Número/Paginação/Ano: v. 29, p. 240, res. TW93, 2010
- Conference titles: International Congress on Neuromuscular Diseases (ICNMD)
-
ABNT
GURGEL-GIANNETTI, Juliana et al. Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 2010 -
APA
Gurgel-Giannetti, J., Lara, M. T., Concentino, E. L. C., Martins-Machado, M. C. P., Yamamoto, L. U., Onofre-Oliveira, P., & Vainzof, M. (2010). Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. -
NLM
Gurgel-Giannetti J, Lara MT, Concentino ELC, Martins-Machado MCP, Yamamoto LU, Onofre-Oliveira P, Vainzof M. Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. 2010 ; 29 240.[citado 2024 nov. 12 ] -
Vancouver
Gurgel-Giannetti J, Lara MT, Concentino ELC, Martins-Machado MCP, Yamamoto LU, Onofre-Oliveira P, Vainzof M. Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. 2010 ; 29 240.[citado 2024 nov. 12 ] - 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017
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