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The STEP program included four phase 3 clinical trials with over 4,500 participants
Primary carnitine deficiency is a genetic disorder of the cellular carnitine-transporter system that typically appears by the age of five with symptoms of cardiomyopathy, skeletal-muscle weakness, and hypoglycemia
If your levels are already normal, your body will just excrete excess since B12 is water soluble
All participants were white
It also contains sodium chloride 9.0mg and 1N acetic acid, and water
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