A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels (2016)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1016/j.pediatrneurol.2016.01.023
- Subjects: DOENÇAS CONGÊNITAS; MUTAÇÃO GENÉTICA; MIOPIA; BRASILEIROS
- Language: Inglês
- Imprenta:
- Publisher place: Chippewa Falls (US)
- Date published: 2016
- Source:
- Título do periódico: Pediatric Neurology
- ISSN: 0887-8994
- Volume/Número/Paginação/Ano: v. 58, p. 107-112, 2016
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ABATH NETO, Osorio et al. A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels. Pediatric Neurology, v. 58, p. 107-112, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2016.01.023. Acesso em: 23 abr. 2024. -
APA
Abath Neto, O., Silva, M. R. e, Martins, C. de A., Oliveira, A. de S. B., Reed, U. C., Biancalana, V., et al. (2016). A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels. Pediatric Neurology, 58, 107-112. doi:10.1016/j.pediatrneurol.2016.01.023 -
NLM
Abath Neto O, Silva MR e, Martins C de A, Oliveira A de SB, Reed UC, Biancalana V, Pesquero JB, Laporte J, Zanoteli E. A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels [Internet]. Pediatric Neurology. 2016 ; 58 107-112.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2016.01.023 -
Vancouver
Abath Neto O, Silva MR e, Martins C de A, Oliveira A de SB, Reed UC, Biancalana V, Pesquero JB, Laporte J, Zanoteli E. A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels [Internet]. Pediatric Neurology. 2016 ; 58 107-112.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2016.01.023 - Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement
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Informações sobre o DOI: 10.1016/j.pediatrneurol.2016.01.023 (Fonte: oaDOI API)
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