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Description
There have been reported at least 15 syndromes in which carnitine deficiency seems to be secondary to genetic defects of intermediary metabolism or to other conditions [40]

Date published: 2020-07-21 Rated 5 out of 5 by Miriam S

Form: Multidose vial for reconstitution

In June 2016, the first EPP patients received the drug under the approval
