P48 Genetic and functional investigation of Brown-Vialetto-Van Laere syndrome and related neuropathies

MLA

Mary M. Reilly, et al. “P48 Genetic and Functional Investigation of Brown-Vialetto-Van Laere Syndrome and Related Neuropathies.” Neuromuscular Disorders, vol. 22, Mar. 2012, pp. S19–20. EBSCOhost, https://doi.org/10.1016/s0960-8966(12)70056-1.

APA

Mary M. Reilly, Francesco Muntoni, H Houlden, Peter E. Clayton, John M. Land, A.B. Singleton, Iain P. Hargreaves, Janel O. Johnson, Amelie Pandraud, & A.R. Foley. (2012). P48 Genetic and functional investigation of Brown-Vialetto-Van Laere syndrome and related neuropathies. Neuromuscular Disorders, 22, S19–S20. https://doi.org/10.1016/s0960-8966(12)70056-1

Chicago

Mary M. Reilly, Francesco Muntoni, H Houlden, Peter E. Clayton, John M. Land, A.B. Singleton, Iain P. Hargreaves, Janel O. Johnson, Amelie Pandraud, and A.R. Foley. 2012. “P48 Genetic and Functional Investigation of Brown-Vialetto-Van Laere Syndrome and Related Neuropathies.” Neuromuscular Disorders 22 (March): S19–20. doi:10.1016/s0960-8966(12)70056-1.