APA (7th ed.) Citation

Ben Yaou, R., Gerard, M., Chami, K., Sehier, A., Belin, A., Labombarda, F., . . . Chapon, F. (2014). G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features. Neuromuscular Disorders, 24(9/10), 843. https://doi.org/10.1016/j.nmd.2014.06.172

Chicago Style (17th ed.) Citation

Ben Yaou, R., et al. "G.P.142: A New EMD Gene Missense Mutation in Exon 1 Leads to Absence of Emerin and Is Responsible for X-linked Dilated Cardiomyopathy with Conduction Defects and Arrhythmias and Almost Elusive Skeletal Muscle Features." Neuromuscular Disorders 24, no. 9/10 (2014): 843. https://doi.org/10.1016/j.nmd.2014.06.172.

MLA (9th ed.) Citation

Ben Yaou, R., et al. "G.P.142: A New EMD Gene Missense Mutation in Exon 1 Leads to Absence of Emerin and Is Responsible for X-linked Dilated Cardiomyopathy with Conduction Defects and Arrhythmias and Almost Elusive Skeletal Muscle Features." Neuromuscular Disorders, vol. 24, no. 9/10, 2014, p. 843, https://doi.org/10.1016/j.nmd.2014.06.172.