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Q38779251-F827B057-0EF9-41D6-AC8D-D40F7DA59CB0
Q38779251-F827B057-0EF9-41D6-AC8D-D40F7DA59CB0
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Statement
http://www.wikidata.org/entity/statement/Q38779251-F827B057-0EF9-41D6-AC8D-D40F7DA59CB0
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy.
P2860
Q38779251-F827B057-0EF9-41D6-AC8D-D40F7DA59CB0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38779251-F827B057-0EF9-41D6-AC8D-D40F7DA59CB0
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wasDerivedFrom
ac3dd4d8b2fcb214915c163d29ef5dfeea6f712a
P2860
Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndrome