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malonyl CoA
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OMIM - Congenital disorder
Livers from high-fat fed rats treated with Acetyl-CoA carboxylase inhibitor
Neural stem cells sorted for SPOT14-positive and negative populations
Synthetic metabolic circuit with isocitrate lyase and malate synthase alters fatty acid metabolism
Impact of sesamin, episesamin and sesamolin in rat hepatic gene expression profiles.
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Literature
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Malonyl coenzyme A decarboxylase deficiency with a novel mutation.
Heterogenous Clinical Landscape in a Consanguineous Malonic Aciduria Family.
3D-QSAR analysis of MCD inhibitors by CoMFA and CoMSIA.
Chemical-genetic induction of Malonyl-CoA decarboxylase in skeletal muscle.
A Korean child diagnosed with malonic aciduria harboring a novel start codon mutation following pres…
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Clinical Trials
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Muscle Malonyl Coa Biomarker Assay Development
Metabolic Response to Fat and Glucose
Combined Malonic and Methylmalonic Aciduria (CMAMMA): Gene Identification and Outcome Study
Lactate Profile and Fat Oxidation During Exercise
Study of Dapagliflozin on Mitochondrial Dysfunction and Impaired Insulin Signaling/Action
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