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• W2023484190 startingPage "38" @default.
• W2023484190 abstract "Abstract Current knowledge of the metabolic role, biosynthesis, cellular uptake, excretion and turnover of carnitine is reviewed. The clinical spectrum and possible aetiology of the primary muscle and primary systemic carnitine deficiency syndromes are considered and the various genetic defects of intermediary metabolism which can give rise to secondary carnitine deficiency are indicated." @default.
• W2023484190 created "2016-06-24" @default.
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• W2023484190 date "1984-03-01" @default.
• W2023484190 modified "2023-10-02" @default.
• W2023484190 title "Carnitine metabolism and inborn errors" @default.
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• W2023484190 doi "https://doi.org/10.1007/bf03047372" @default.
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