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Q22008704-BAA5D20C-FD2D-450E-A9B8-7D9ECAEDD4D3
Q22008704-BAA5D20C-FD2D-450E-A9B8-7D9ECAEDD4D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-BAA5D20C-FD2D-450E-A9B8-7D9ECAEDD4D3
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P2860
Q22008704-BAA5D20C-FD2D-450E-A9B8-7D9ECAEDD4D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-BAA5D20C-FD2D-450E-A9B8-7D9ECAEDD4D3
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wasDerivedFrom
e953cef9d302ca1202c790b3d5554b44cbd946c0
P2860
Definition of the locus responsible for systemic carnitine deficiency within a 1.6-cM region of mouse chromosome 11 by detailed linkage analysis.