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Q28119074-0A317B75-1C24-45A0-9818-63D36DEA18C0
Q28119074-0A317B75-1C24-45A0-9818-63D36DEA18C0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28119074-0A317B75-1C24-45A0-9818-63D36DEA18C0
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers
P2860
Q28119074-0A317B75-1C24-45A0-9818-63D36DEA18C0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28119074-0A317B75-1C24-45A0-9818-63D36DEA18C0
rank
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type
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wasDerivedFrom
8ab825b50968bbda9b3f133eb2c9303c220f8e85
P2860
Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome