DOI:
10.1055/s-00000034
Klinische Pädiatrie
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References
Hisahara S, Matsushita T, Furuyama H. et al
A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis.
Tohoku J Exp Med 2015;
235: 305-310
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