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4159822
4159822
https://w3id.org/oc/corpus/br/4159822
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P3181
0eac20e1c4e4edb9ab756988234fc86de512d868
P3181
Q22008704-C06E54A9-6458-4084-9DB0-DE3B0D35F2DA
P3181
4159822
https://w3id.org/oc/corpus/br/4159822