Cite

Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy

MLA

Lakshmi Mehta, et al. “Congenital Disorder of Glycosylation Due to DPM1 Mutations Presenting with Dystroglycanopathy-Type Congenital Muscular Dystrophy.” Molecular Genetics and Metabolism, vol. 110, Nov. 2013, pp. 345–51. EBSCOhost, https://doi.org/10.1016/j.ymgme.2013.06.016.



APA

Lakshmi Mehta, Kevin P. Campbell, Charles J. Waechter, Tobias Willer, Amy Yang, Bobby G. Ng, Jeffrey S. Rush, Kimiyo Raymond, Hudson H. Freeze, & Steven A. Moore. (2013). Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy. Molecular Genetics and Metabolism, 110, 345–351. https://doi.org/10.1016/j.ymgme.2013.06.016



Chicago

Lakshmi Mehta, Kevin P. Campbell, Charles J. Waechter, Tobias Willer, Amy Yang, Bobby G. Ng, Jeffrey S. Rush, Kimiyo Raymond, Hudson H. Freeze, and Steven A. Moore. 2013. “Congenital Disorder of Glycosylation Due to DPM1 Mutations Presenting with Dystroglycanopathy-Type Congenital Muscular Dystrophy.” Molecular Genetics and Metabolism 110 (November): 345–51. doi:10.1016/j.ymgme.2013.06.016.