[Muscular carnitine-palmityl-transferase deficiency]
- PMID: 6861647
- DOI: 10.1055/s-2008-1069692
[Muscular carnitine-palmityl-transferase deficiency]
Abstract
Deficiency in carnitine-palmityl-transferase (CPT) was demonstrated in a 20-year-old man with paroxysmal myoglobinuria, after failure to discover another cause. It is concluded that muscular CPT deficiency must be excluded before a recurrent myoglobinuria is classified as "idiopathic".
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