Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations (2017)
- Autores:
- Autores USP: SOBREIRA, CLAUDIA FERREIRA DA ROSA - FMRP ; MARQUES JÚNIOR, WILSON - FMRP ; BARREIRA, AMILTON ANTUNES - FMRP
- Unidade: FMRP
- Assuntos: MITOCÔNDRIAS; DNA MITOCONDRIAL; PATOLOGIA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Abstracts
- Nome do evento: International Meeting of Mitochondrial Pathology (EUROMIT)
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ABNT
CARVALHO, E. et al. Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. 2017, Anais.. Cologne: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2017. . Acesso em: 26 abr. 2024. -
APA
Carvalho, E., Trindade, K. B. B., Marques Júnior, W., Barreira, A. A., & Sobreira, C. F. da R. (2017). Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. In Abstracts. Cologne: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Carvalho E, Trindade KBB, Marques Júnior W, Barreira AA, Sobreira CF da R. Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. Abstracts. 2017 ;[citado 2024 abr. 26 ] -
Vancouver
Carvalho E, Trindade KBB, Marques Júnior W, Barreira AA, Sobreira CF da R. Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. Abstracts. 2017 ;[citado 2024 abr. 26 ] - Late-onset TTRMET30 famial amyloid polyneuropathy (FAPTTRMET30)
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