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Description
However, carriers of single copies of mutations rarely have noticeable negative effects.[ref] Primary carnitine deficiency: The SLC22A5 gene encodes the carnitine transporter known as OCTN2
J Altern Complement Med
P., Ho, A
Effects of L-propionylcarnitine on ischemia-induced myocardial dysfunction in men with angina pectoris
Conclusion and practical applications A strength of our study was the duration of the intervention
