Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions (2017)
- Authors:
- USP affiliated authors: SOBREIRA, CLAUDIA FERREIRA DA ROSA - FMRP ; ESCARSO, SILVIA HELENA ANDRIÃO - FMRP ; MARQUES JÚNIOR, WILSON - FMRP
- Unidade: FMRP
- Subjects: OFTALMOPATIAS; MITOCÔNDRIAS; MUTAÇÃO GENÉTICA; DNA MITOCONDRIAL
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: International Meeting of Mitochondrial Pathology (EUROMIT)
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ABNT
SOBREIRA, Cláudia Ferreira da Rosa et al. Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions. 2017, Anais.. Cologne: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2017. . Acesso em: 29 dez. 2025. -
APA
Sobreira, C. F. da R., Carvalho, E. H. T., Escarso, S. H. A., Toledo, F. O., Trindade, K. B. B., Reis, F. H. Z., & Marques Júnior, W. (2017). Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions. In Abstracts. Cologne: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Sobreira CF da R, Carvalho EHT, Escarso SHA, Toledo FO, Trindade KBB, Reis FHZ, Marques Júnior W. Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions. Abstracts. 2017 ;[citado 2025 dez. 29 ] -
Vancouver
Sobreira CF da R, Carvalho EHT, Escarso SHA, Toledo FO, Trindade KBB, Reis FHZ, Marques Júnior W. Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions. Abstracts. 2017 ;[citado 2025 dez. 29 ] - Clinical phenotipes of primary coenzyme Q10 deficiency
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