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[DOI] [PubMed] [Google Scholar] 78.Higuchi T., Abe M., Yamazaki T., Okawa E., Ando H., Hotta S., Oikawa O., Kikuchi F., Okada K., Soma M

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There are three main phenotypes of primary carnitine deficiency (PCD): the fatal neonatal form, the severe infantile hepatocardiomuscular form and the most common (and mildest) myopathic form, characterised by exercise-induced muscle pain, weakness and myoglobinuria