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OCTN2 ) mutations, typically manifests in children aged 17 years, with a frequency of 15 per 10.000 and causes metabolic derangements including hypoketotic hypoglycemia, hepatic steatosis, myopathy, and potentially sudden death due to cardiomyopathy [4, 6]

Informao nutricional Ingredientes gua deionizada, L-carnitina, mix de vitaminas (pantotenato de clcio (vitamina B5) e tiamina (vitamina B1)), espessante glicerina vegetal, acidulantes cido ctrico e cido mlico, conservantes sorbato de potssio e benzoato de sdio e aromatizante

DOI: 10.1016/j.jad.2018.04.111

(2021) Response to Electrostimulation Is Impaired in Muscle Cells from Patients with Chronic Obstructive Pulmonary Disease