Fatal cardiomyopathy associated with 3‐hydroxy‐3‐methylglutaryl‐CoA lyase deficiency
- 1 May 1994
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 17 (3) , 291-294
- https://doi.org/10.1007/bf00711810
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
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- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new casesClinical Chemistry, 1990
- 3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric methodClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- 3‐hydroxy‐3‐methylglutaryl‐coenzyme a lyase deficiency: Report of five new patientsJournal of Inherited Metabolic Disease, 1986