A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene (Q44272889)

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A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene
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    A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene (English)

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