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Q24530714-41F4D1FC-9D8E-4390-B406-9E3C711027E3
Q24530714-41F4D1FC-9D8E-4390-B406-9E3C711027E3
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Statement
http://www.wikidata.org/entity/statement/Q24530714-41F4D1FC-9D8E-4390-B406-9E3C711027E3
Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome.
P2860
Q24530714-41F4D1FC-9D8E-4390-B406-9E3C711027E3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24530714-41F4D1FC-9D8E-4390-B406-9E3C711027E3
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wasDerivedFrom
449ccec4c8ae3839a5bc9796d86b9980f93b248d
P2860
Channelopathies: Kir2.1 mutations jeopardize many cell functions.