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Conboy E, Vairo F, Schultz M, et al. Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. JIMD Rep. 2017;40:63-69doi: 10.1007/8904_2017_59.
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, 4063-69. https://doi.org/10.1007/8904_2017_59
Conboy, Erin, et al. "Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features." JIMD reports vol. 40 (2018): 63-69. doi: https://doi.org/10.1007/8904_2017_59
Conboy E, Vairo F, Schultz M, Agre K, Ridsdale R, Deyle D, Oglesbee D, Gavrilov D, Klee EW, Lanpher B. Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. JIMD Rep. 2018;40:63-69. doi: 10.1007/8904_2017_59. Epub 2017 Oct 14. PMID: 29030856; PMCID: PMC6122033.
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