Subjects: MUTAÇÃO GENÉTICA, MIOPATIAS CONGÊNITAS ESTRUTURAIS, DOENÇAS NEUROMUSCULARES, PROTEÍNAS MUSCULARES
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MOKBEL, Nancy et al. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. Brain, v. 136, n. 2, p. 494-507, 2013Tradução . . Disponível em: https://doi.org/10.1093/brain/aws348. Acesso em: 24 ago. 2024.APA
Mokbel, N., Ilkovski, B., Kreissl, M., Memo, M., Jeffries, C. M., Marttila, M., et al. (2013). K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. Brain, 136( 2), 494-507. doi:10.1093/brain/aws348NLM
Mokbel N, Ilkovski B, Kreissl M, Memo M, Jeffries CM, Marttila M, Lehtokari V-L, Lemola E, Grönholm M, Yang N, Menard D, Marcorelles P, Echaniz-Laguna A, Reimann J, Vainzof M, Monnier N, Ravenscroft G, McNamara E, Nowak KJ, Laing NG, Wallgren-Pettersson C, Trewhella J, Marston S, Ottenheijm C, North KN, Clarke NF. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity [Internet]. Brain. 2013 ; 136( 2): 494-507.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1093/brain/aws348Vancouver
Mokbel N, Ilkovski B, Kreissl M, Memo M, Jeffries CM, Marttila M, Lehtokari V-L, Lemola E, Grönholm M, Yang N, Menard D, Marcorelles P, Echaniz-Laguna A, Reimann J, Vainzof M, Monnier N, Ravenscroft G, McNamara E, Nowak KJ, Laing NG, Wallgren-Pettersson C, Trewhella J, Marston S, Ottenheijm C, North KN, Clarke NF. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity [Internet]. Brain. 2013 ; 136( 2): 494-507.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1093/brain/aws348