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Q30837035-9F94AFBF-26D6-4B43-984E-0BAE2948AC1F
Q30837035-9F94AFBF-26D6-4B43-984E-0BAE2948AC1F
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Statement
http://www.wikidata.org/entity/statement/Q30837035-9F94AFBF-26D6-4B43-984E-0BAE2948AC1F
Localization of organic cation/carnitine transporter (OCTN2) in cells forming the blood-brain barrier.
P2860
Q30837035-9F94AFBF-26D6-4B43-984E-0BAE2948AC1F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30837035-9F94AFBF-26D6-4B43-984E-0BAE2948AC1F
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type
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wasDerivedFrom
312b1385f3680f71cd6f87dfa6138a20339bf8d9
P2860
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter