Mokbel, N.; Ilkovski, B; Memo, M.; Vainzof, Mariz 
Source: Neuromuscular Disorders. Conference titles: International Congress of The World Muscle Society. Unidade: IB
Subjects: GENÉTICA, GENOMAS, DISTROFIA MUSCULAR
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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: 28 abr. 2026. , 2012APA
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.2012.06.143NLM
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 2026 abr. 28 ] Available from: https://doi.org/10.1016/j.nmd.2012.06.143Vancouver
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 2026 abr. 28 ] Available from: https://doi.org/10.1016/j.nmd.2012.06.143
