Short-chain enoyl-CoA hydratase (ECHS1) is a multifunctional mitochondrial matrix enzyme that is involved in the oxidation of fatty acids and
Author: nemadmin
Mitochondrial Fatty Acid Oxidation Disorders Associated with Short-Chain Enoyl-CoA Hydratase (ECHS1) DeficiencyMitochondrial Fatty Acid Oxidation Disorders Associated with Short-Chain Enoyl-CoA Hydratase (ECHS1) Deficiency
Mitochondrial fatty acid -oxidation (FAO) is the primary pathway for fatty acid metabolism in humans, performing a key role in
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Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency (ECHS1)Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency (ECHS1)
Clinical characteristics. Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency (ECHS1D) represents a clinical spectrum in which several phenotypes have been described:
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Clinical, biochemical, and genetic features of four patients with ECHS1Clinical, biochemical, and genetic features of four patients with ECHS1
Short‐chain enoyl‐CoA hydratase (SCEH or ECHS1) deficiency is a rare inborn error of metabolism caused by biallelic mutations in the