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Q28142569-B5C665F3-3B7B-4806-A271-518BBE0AD1EE
Q28142569-B5C665F3-3B7B-4806-A271-518BBE0AD1EE
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Statement
http://www.wikidata.org/entity/statement/Q28142569-B5C665F3-3B7B-4806-A271-518BBE0AD1EE
Functional characteristics and tissue distribution pattern of organic cation transporter 2 (OCTN2), an organic cation/carnitine transporter
P2860
Q28142569-B5C665F3-3B7B-4806-A271-518BBE0AD1EE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28142569-B5C665F3-3B7B-4806-A271-518BBE0AD1EE
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type
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Statement
wasDerivedFrom
bdf4ecf2e78804e8d3dcb286f76037035d8aab1b
P2860
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter