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Clinical relevance of skeletal muscle abnormalities in patients with cirrhosis
Precautions and safety tips Always read the instructions given on the label and take the recommended dosage
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(PubMed) Buhling K, Schumacher A, Eulenburg CZ, Laakmann E
Hereditary causes include genetic defects in the metabolism of amino acids, cholesterol, and fatty acids, such as propionyl-CoA carboxylase deficiency (aka propionic acidemia) and medium chain acyl-CoA dehydrogenase deficiency (36)
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