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5030
5030
http://dx.doi.org/10.1038/5030
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P356
Q22008704-59F0EBAC-072C-4B91-82BE-9E599EA250C1
P356
5030
http://dx.doi.org/10.1038/5030