Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course (2009)
- Authors:
- USP affiliated authors: SOBREIRA, CLAUDIA FERREIRA DA ROSA - FMRP ; MARQUES JÚNIOR, WILSON - FMRP ; SANTOS, ANTONIO CARLOS DOS - FMRP ; PINA NETO, JOÃO MONTEIRO DE - FMRP ; BARREIRA, AMILTON ANTUNES - FMRP
- Unidade: FMRP
- DOI: 10.1016/j.jns.2008.11.023
- Subjects: NEUROLOGIA; MUTAÇÃO GENÉTICA; MITOCÔNDRIAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of the Neurological Sciences
- ISSN: 0022-510X
- Volume/Número/Paginação/Ano: v. 278, n. 1-2, p. 132-134, 2009
- Status:
- Nenhuma versão em acesso aberto identificada
-
ABNT
SOBREIRA, Cláudia Ferreira da Rosa et al. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course. Journal of the Neurological Sciences, v. 278, n. 1-2, p. 132-134, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jns.2008.11.023. Acesso em: 02 abr. 2026. -
APA
Sobreira, C. F. da R., Marques Júnior, W., Pontes-Neto, O. M., Santos, A. C. dos, Pina Neto, J. M. de, & Barreira, A. A. (2009). Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course. Journal of the Neurological Sciences, 278( 1-2), 132-134. doi:10.1016/j.jns.2008.11.023 -
NLM
Sobreira CF da R, Marques Júnior W, Pontes-Neto OM, Santos AC dos, Pina Neto JM de, Barreira AA. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course [Internet]. Journal of the Neurological Sciences. 2009 ; 278( 1-2): 132-134.[citado 2026 abr. 02 ] Available from: https://doi.org/10.1016/j.jns.2008.11.023 -
Vancouver
Sobreira CF da R, Marques Júnior W, Pontes-Neto OM, Santos AC dos, Pina Neto JM de, Barreira AA. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course [Internet]. Journal of the Neurological Sciences. 2009 ; 278( 1-2): 132-134.[citado 2026 abr. 02 ] Available from: https://doi.org/10.1016/j.jns.2008.11.023 - Increasing the differential diagnosis of the inherited demyelinating neuropathies with non-uniform nerve conduction(NCS): Andermann syndrome
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