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Description
Hereditary or acquired defects in the transport mechanisms are the major cause of l-carnitine deficiency, leading to pathologies such as cardiomyopathy and skeletal muscle myopathy [12,13]

Here we describe that reduced C/EBP LIP expression due to genetic ablation of the uORF delays the development of age-associated phenotypes in mice

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10.1111/j.1755-148X.2009.00610.x (2009)

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