Rumpf K W, Kaiser H, Goebel H H, Wagner H A, Ullmann B, DiMauro S, Scheler F
Dtsch Med Wochenschr. 1983 Jul 8;108(27):1058-61. doi: 10.1055/s-2008-1069692.
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".