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Q36682239-655D7A0F-EA2A-48A7-883E-623A7CC2ABC9
Q36682239-655D7A0F-EA2A-48A7-883E-623A7CC2ABC9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36682239-655D7A0F-EA2A-48A7-883E-623A7CC2ABC9
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome
P2860
Q36682239-655D7A0F-EA2A-48A7-883E-623A7CC2ABC9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36682239-655D7A0F-EA2A-48A7-883E-623A7CC2ABC9
rank
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type
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Statement
wasDerivedFrom
d1f6de3a6ca3475207b9c24cd02f887a54b14664
P2860
Transcription factor Sox11 is essential for both embryonic and adult neurogenesis.