Clinical and molecular findings in a cohort of ANO5-related myopathy (2019)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1002/acn3.50801
- Subjects: DISTROFIA MUSCULAR; PROTEÍNAS DA MEMBRANA; PROTEÍNAS DE TRANSPORTE; MUTAÇÃO GENÉTICA; DIAGNÓSTICO HISTOLÓGICO; RESSONÂNCIA MAGNÉTICA; ANÁLISE DE SEQUÊNCIA DE DNA
- Language: Inglês
- Imprenta:
- Source:
- Título: Annals of clinical and translational neurology
- ISSN: 2328-9503
- Volume/Número/Paginação/Ano: v. 6, n. 7, p. 1225-1238, 2019
- Status:
- Artigo publicado em periódico de acesso aberto (Gold Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
SILVA, Andre M. S et al. Clinical and molecular findings in a cohort of ANO5-related myopathy. Annals of clinical and translational neurology, v. 6, n. 7, p. 1225-1238, 2019Tradução . . Disponível em: https://doi.org/10.1002/acn3.50801. Acesso em: 07 abr. 2026. -
APA
Silva, A. M. S., Coimbra-neto, A. R., Souza, P. V. S., Winckler, P. B., Goncalves, M. V. M., Cavalcanti, E. B. U., et al. (2019). Clinical and molecular findings in a cohort of ANO5-related myopathy. Annals of clinical and translational neurology, 6( 7), 1225-1238. doi:10.1002/acn3.50801 -
NLM
Silva AMS, Coimbra-neto AR, Souza PVS, Winckler PB, Goncalves MVM, Cavalcanti EBU, Carvalho AADS, Sobreire CFDR, Reed UC, Zanoteli E. Clinical and molecular findings in a cohort of ANO5-related myopathy [Internet]. Annals of clinical and translational neurology. 2019 ; 6( 7): 1225-1238.[citado 2026 abr. 07 ] Available from: https://doi.org/10.1002/acn3.50801 -
Vancouver
Silva AMS, Coimbra-neto AR, Souza PVS, Winckler PB, Goncalves MVM, Cavalcanti EBU, Carvalho AADS, Sobreire CFDR, Reed UC, Zanoteli E. Clinical and molecular findings in a cohort of ANO5-related myopathy [Internet]. Annals of clinical and translational neurology. 2019 ; 6( 7): 1225-1238.[citado 2026 abr. 07 ] Available from: https://doi.org/10.1002/acn3.50801 - Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
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