Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy (2019)
- Authors:
- Autor USP: ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1007/s00401-019-02034-8
- Subjects: MIOPATIAS CONGÊNITAS ESTRUTURAIS; DOENÇAS MUSCULOSQUELÉTICAS; CITOESQUELETO; MEMBRANA NUCLEAR
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Acta neuropathologica
- ISSN: 0001-6322
- Volume/Número/Paginação/Ano: v. 138, n. 3, Special Issue, p. 477-495, 2019
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by
-
ABNT
ROSS, Jacob A et al. Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy. Acta neuropathologica, v. 138, n. 3, p. 477-495, 2019Tradução . . Disponível em: https://doi.org/10.1007/s00401-019-02034-8. Acesso em: 24 abr. 2024. -
APA
Ross, J. A., Levy, Y., Ripolone, M., Kolb, J. S., Turmaine, M., Holt, M., et al. (2019). Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy. Acta neuropathologica, 138( 3), 477-495. doi:10.1007/s00401-019-02034-8 -
NLM
Ross JA, Levy Y, Ripolone M, Kolb JS, Turmaine M, Holt M, Lindqvist J, Claeys KG, Weis J, Zanoteli E. Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy [Internet]. Acta neuropathologica. 2019 ; 138( 3): 477-495.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1007/s00401-019-02034-8 -
Vancouver
Ross JA, Levy Y, Ripolone M, Kolb JS, Turmaine M, Holt M, Lindqvist J, Claeys KG, Weis J, Zanoteli E. Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy [Internet]. Acta neuropathologica. 2019 ; 138( 3): 477-495.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1007/s00401-019-02034-8 - Myopathy due to HMGCR antibodies in adult mimicking muscular dystrophy associated with cancer and statin exposure - narrative review of the literature - case report
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Informações sobre o DOI: 10.1007/s00401-019-02034-8 (Fonte: oaDOI API)
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