Mevalonic aciduria in 3 siblings: A new recognizable metabolic encephalopathy
- 30 June 1993
- journal article
- case report
- Published by Elsevier in Pediatric Neurology
- Vol. 9 (3) , 243-246
- https://doi.org/10.1016/0887-8994(93)90095-t
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Mevalonic aciduria: Family studies in mevalonate kinase deficiency, an inborn error of cholesterol biosynthesisJournal of Inherited Metabolic Disease, 1987
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- Mevalonic aciduria: an inborn error of cholesterol biosynthesis?Clinica Chimica Acta; International Journal of Clinical Chemistry, 1985