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5030
5030
https://scigraph.springernature.com/pub.10.1038/5030
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P2888
Q22008704-67039A28-536B-438A-BD38-829DFAF10E19
P2888
5030
https://scigraph.springernature.com/pub.10.1038/5030