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Q37604522-FAC5E30C-1F99-41BE-8F26-F841EECF9F8F
Q37604522-FAC5E30C-1F99-41BE-8F26-F841EECF9F8F
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http://www.wikidata.org/entity/statement/Q37604522-FAC5E30C-1F99-41BE-8F26-F841EECF9F8F
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy
P2860
Q37604522-FAC5E30C-1F99-41BE-8F26-F841EECF9F8F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37604522-FAC5E30C-1F99-41BE-8F26-F841EECF9F8F
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wasDerivedFrom
41d9ded46f5ecb3d2f4469c106a2abed4a915102
P2860
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome