Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Clinical Course and Description of Causal Mutations in Two Patients
Open Access
- 1 March 2001
- journal article
- case report
- Published by Springer Nature in Pediatric Research
- Vol. 49 (3) , 326-331
- https://doi.org/10.1203/00006450-200103000-00005
Abstract
No abstract availableKeywords
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