secondary l-carnitine deficiency

secondary l-carnitine deficiency Primary vs Carnitine Explained Disorders of mitochondrial long-chain fatty

Name: secondary l-carnitine deficiency Primary vs Carnitine Explained Disorders of mitochondrial long-chain fatty
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SKU: 80936973125
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Disorders of mitochondrial long chain fatty acid oxidation and the carnitine shuttle Reviews in Endocrine and Metabolic Disorders Springer Nature Link The Role of L Carnitine in Kidney Disease and Related Metabolic Dysfunctions Carnitine: Genetic Variants Affecting Mitochondrial Energy and Health Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2020;25:23 29]

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Description

It is a soluble protein that acts as a VEGF receptor decoy by combining ligand-binding elements of the extracellular domains of VEGFR1 and two fused to the constant region (Fc) of the immunoglobulin G (IgG)