Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations

MLA

Denis Oriot, et al. “Novel Molecular Diagnostic Approaches for X-Linked Centronuclear (Myotubular) Myopathy Reveal Intronic Mutations.” Neuromuscular Disorders, vol. 20, June 2010, pp. 375–81. EBSCOhost, https://doi.org/10.1016/j.nmd.2010.03.015.

APA

Denis Oriot, Christine Kretz, Carsten G. Bönnemann, Nicolas Dondaine, Valérie Tosch, Nasim Vasli, Norma B. Romero, Anne-Sophie Nicot, Jocelyn Laporte, Gilles Duval, Valérie Biancalana, Claire Gasnier, Magalie Barth, Hugues Puissant, & Betty Heller. (2010). Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations. Neuromuscular Disorders, 20, 375–381. https://doi.org/10.1016/j.nmd.2010.03.015

Chicago

Denis Oriot, Christine Kretz, Carsten G. Bönnemann, Nicolas Dondaine, Valérie Tosch, Nasim Vasli, Norma B. Romero, et al. 2010. “Novel Molecular Diagnostic Approaches for X-Linked Centronuclear (Myotubular) Myopathy Reveal Intronic Mutations.” Neuromuscular Disorders 20 (June): 375–81. doi:10.1016/j.nmd.2010.03.015.