Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE.

MLA

Maselli, R. A., et al. “Congenital Myasthenic Syndrome Associated with Epidermolysis Bullosa Caused by Homozygous Mutations in PLEC1 and CHRNE.” Clinical Genetics, vol. 80, no. 5, Nov. 2011, pp. 444–51. EBSCOhost, https://doi.org/10.1111/j.1399-0004.2010.01602.x.

APA

Maselli, R. A., Arredondo, J., Cagney, O., Mozaffar, T., Skinner, S., Yousif, S., Davis, R. R., Gregg, J. P., Sivak, M., Konia, T. H., Thomas, K., & Wollmann, R. L. (2011). Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE. Clinical Genetics, 80(5), 444–451. https://doi.org/10.1111/j.1399-0004.2010.01602.x

Chicago

Maselli, R A, J Arredondo, O Cagney, T Mozaffar, S Skinner, S Yousif, R R Davis, et al. 2011. “Congenital Myasthenic Syndrome Associated with Epidermolysis Bullosa Caused by Homozygous Mutations in PLEC1 and CHRNE.” Clinical Genetics 80 (5): 444–51. doi:10.1111/j.1399-0004.2010.01602.x.