K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity (2012)
- Authors:
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- DOI: 10.1016/j.nmd.2012.06.143
- Subjects: GENÉTICA; GENOMAS; DISTROFIA MUSCULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 22, n. 9-10, oct. p. 845, G.P. 15, 2012
- Conference titles: International Congress of The World Muscle Society
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MOKBEL, N. et al. K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2012.06.143. Acesso em: 19 abr. 2024. , 2012 -
APA
Mokbel, N., Ilkovski, B., Memo, M., & Vainzof, M. (2012). K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2012.06.143 -
NLM
Mokbel N, Ilkovski B, Memo M, Vainzof M. K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity [Internet]. Neuromuscular Disorders. 2012 ; 22( 9-10): oct. 845.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.nmd.2012.06.143 -
Vancouver
Mokbel N, Ilkovski B, Memo M, Vainzof M. K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity [Internet]. Neuromuscular Disorders. 2012 ; 22( 9-10): oct. 845.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.nmd.2012.06.143 - Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta]
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Informações sobre o DOI: 10.1016/j.nmd.2012.06.143 (Fonte: oaDOI API)
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