Miller, B., Freeze, H. H., Hoffmann, G. F., & Sarafoglou, K. (2011). Pubertal development in ALG6 deficiency (congenital disorder of glycosylation type Ic). Molecular genetics and metabolism, 103(1), . https://doi.org/10.1016/j.ymgme.2011.01.016
Chicago Style (17th ed.) CitationMiller, Bradley, Hudson H. Freeze, Georg F. Hoffmann, and Kyriakie Sarafoglou. "Pubertal Development in ALG6 Deficiency (congenital Disorder of Glycosylation Type Ic)." Molecular Genetics and Metabolism 103, no. 1 (2011). https://doi.org/10.1016/j.ymgme.2011.01.016.
MLA (9th ed.) CitationMiller, Bradley, et al. "Pubertal Development in ALG6 Deficiency (congenital Disorder of Glycosylation Type Ic)." Molecular Genetics and Metabolism, vol. 103, no. 1, 2011, https://doi.org/10.1016/j.ymgme.2011.01.016.