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Q47113019-1E17DB79-4841-427F-AEB9-B17F11A65BA6
Q47113019-1E17DB79-4841-427F-AEB9-B17F11A65BA6
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http://www.wikidata.org/entity/statement/Q47113019-1E17DB79-4841-427F-AEB9-B17F11A65BA6
A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
P2860
Q47113019-1E17DB79-4841-427F-AEB9-B17F11A65BA6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47113019-1E17DB79-4841-427F-AEB9-B17F11A65BA6
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wasDerivedFrom
5b931c88c21682ba2605c5c91a4ad64729c32aa0
P2860
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype