Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia

MLA

Munot, P., et al. “Congenital Fibre Type Disproportion Associated with Mutations in the Tropomyosin 3 (TPM3) Gene Mimicking Congenital Myasthenia.” Neuromuscular Disorders, vol. 20, no. 12, Dec. 2010, pp. 796–800. EBSCOhost, https://doi.org/10.1016/j.nmd.2010.07.274.

APA

Munot, P., Lashley, D., Jungbluth, H., Feng, L., Pitt, M., Robb, S. A., Palace, J., Jayawant, S., Kennet, R., Beeson, D., Cullup, T., Abbs, S., Laing, N., Sewry, C., & Muntoni, F. (2010). Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia. Neuromuscular Disorders, 20(12), 796–800. https://doi.org/10.1016/j.nmd.2010.07.274

Chicago

Munot, P., D. Lashley, H. Jungbluth, L. Feng, M. Pitt, S.A. Robb, J. Palace, et al. 2010. “Congenital Fibre Type Disproportion Associated with Mutations in the Tropomyosin 3 (TPM3) Gene Mimicking Congenital Myasthenia.” Neuromuscular Disorders 20 (12): 796–800. doi:10.1016/j.nmd.2010.07.274.