G.P.271: Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies.

MLA

Marttila, M., et al. “G.P.271: Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies.” Neuromuscular Disorders, vol. 24, no. 9/10, Oct. 2014, p. 898. EBSCOhost, https://doi.org/10.1016/j.nmd.2014.06.347.

APA

Marttila, M., Lehtokari, V. L., Marston, S. B., Nyman, T. A., Barnerias, C., Beggs, A. H., Bertin, E., Ceyhan-Birsoy, Ö., Cintas, P., Gerard, M., Gilbert-Dussardier, B., Hogue, J. S., Longman, C., Eymard, B., Frydman, M., Kang, P. B., Klinge, L., Kolski, H., Lochmüller, H., & Magy, L. (2014). G.P.271: Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies. Neuromuscular Disorders, 24(9/10), 898. https://doi.org/10.1016/j.nmd.2014.06.347

Chicago

Marttila, M., V.L. Lehtokari, S.B. Marston, T.A. Nyman, C. Barnerias, A.H. Beggs, E. Bertin, et al. 2014. “G.P.271: Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies.” Neuromuscular Disorders 24 (9/10): 898. doi:10.1016/j.nmd.2014.06.347.