Findings from the individualized management of a patient with Acyl-CoA Oxidase-1 (ACOX1) deficiency: A bedside-to-bench-to-bedside strategy

Acyl-CoA Oxidase-1 (ACOX1) deficiency (MIM 264470) is an autosomal recessive disease characterized by impairments in the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs, which is the first step in the catalysis of the β-oxidative breakdown of very long chain fatty acids (VLCFA) occuring in peroxisom...

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Veröffentlicht in:Molecular genetics and metabolism 2024-11, Vol.143 (3), p.108581, Article 108581
Hauptverfasser: Moreau, Camille, Paquot, Adrien, Ares, Gustavo Soto, Dessein, Anne-Frédérique, Deprez, Benoit, Beghyn, Terence, Dobbelaere, Dries
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Sprache:eng
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