Molecular Heterogeneity in Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Causing Pediatric Cardiomyopathy and Sudden Death
- 16 March 1999
- journal article
- other
- Published by Wolters Kluwer Health in Circulation
- Vol. 99 (10) , 1337-1343
- https://doi.org/10.1161/01.cir.99.10.1337
Abstract
Background—Genetic defects are being increasingly recognized in the etiology of primary cardiomyopathy (CM). Very-long-chain acyl-CoA dehydrogenase (VLCAD) catalyzes the first step in the β-oxidati...Keywords
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