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Q22008704-67D4EFDF-2C7A-460F-BDED-C2BD4E930B46
Q22008704-67D4EFDF-2C7A-460F-BDED-C2BD4E930B46
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-67D4EFDF-2C7A-460F-BDED-C2BD4E930B46
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P2860
Q22008704-67D4EFDF-2C7A-460F-BDED-C2BD4E930B46
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-67D4EFDF-2C7A-460F-BDED-C2BD4E930B46
rank
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Statement
wasDerivedFrom
e953cef9d302ca1202c790b3d5554b44cbd946c0
P2860
The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiologic features.