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Q24622660-EDF1EE11-2FA2-4C7A-A2DF-F8014BE73BDB
Q24622660-EDF1EE11-2FA2-4C7A-A2DF-F8014BE73BDB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24622660-EDF1EE11-2FA2-4C7A-A2DF-F8014BE73BDB
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome
P2860
Q24622660-EDF1EE11-2FA2-4C7A-A2DF-F8014BE73BDB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24622660-EDF1EE11-2FA2-4C7A-A2DF-F8014BE73BDB
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wasDerivedFrom
3084012b18c147dd574649f1dce183a960b69ee4
P2860
Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways