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Q22008704-5489D33B-07E2-43A7-B8D0-FD1CBF5AA447
Q22008704-5489D33B-07E2-43A7-B8D0-FD1CBF5AA447
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-5489D33B-07E2-43A7-B8D0-FD1CBF5AA447
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P2860
Q22008704-5489D33B-07E2-43A7-B8D0-FD1CBF5AA447
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-5489D33B-07E2-43A7-B8D0-FD1CBF5AA447
rank
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Statement
wasDerivedFrom
e953cef9d302ca1202c790b3d5554b44cbd946c0
P2860
Evidence for linkage of human primary systemic carnitine deficiency with D5S436: a novel gene locus on chromosome 5q