APA

Conboy E., Vairo F., Schultz M., Agre K., Ridsdale R., Deyle D., Oglesbee D., Gavrilov D., Klee E. W. & Lanpher B. (2018). Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. : JIMD reports.

Chicago

Conboy Erin, Vairo Filippo, Schultz Matthew, Agre Katherine, Ridsdale Ross, Deyle David, Oglesbee Devin, Gavrilov Dimitar, Klee Eric W and Lanpher Brendan. 2018. Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. : JIMD reports.

Harvard

Conboy E., Vairo F., Schultz M., Agre K., Ridsdale R., Deyle D., Oglesbee D., Gavrilov D., Klee E. W. and Lanpher B. (2018). Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. : JIMD reports.

MLA

Conboy Erin, Vairo Filippo, Schultz Matthew, Agre Katherine, Ridsdale Ross, Deyle David, Oglesbee Devin, Gavrilov Dimitar, Klee Eric W and Lanpher Brendan. Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. : JIMD reports. 2018.