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Q45826766-06CF201A-7808-4473-B54D-153C30708FEB
Q45826766-06CF201A-7808-4473-B54D-153C30708FEB
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Statement
http://www.wikidata.org/entity/statement/Q45826766-06CF201A-7808-4473-B54D-153C30708FEB
Altered synaptobrevin-II trafficking in neurons expressing a synaptophysin mutation associated with a severe neurodevelopmental disorder.
P2860
Q45826766-06CF201A-7808-4473-B54D-153C30708FEB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45826766-06CF201A-7808-4473-B54D-153C30708FEB
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wasDerivedFrom
b20ce28181f4e3ee5161ba053d58370b51462049
P2860
De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy.