Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted mice.
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common inherited disorder of mitochondrial fatty acid beta-oxidation in humans. To better understand the pathogenesis of this disease, we developed a mouse model for MCAD deficiency (MCAD-/-) by gene targeting in embryonic stem (ES) c...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2005-08-01
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Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC1189074?pdf=render |