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Q24600816-4C27F0D8-7878-4C98-9EC9-67E3D820D5D4
Q24600816-4C27F0D8-7878-4C98-9EC9-67E3D820D5D4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24600816-4C27F0D8-7878-4C98-9EC9-67E3D820D5D4
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
P2860
Q24600816-4C27F0D8-7878-4C98-9EC9-67E3D820D5D4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24600816-4C27F0D8-7878-4C98-9EC9-67E3D820D5D4
rank
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type
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Statement
wasDerivedFrom
a461e12bc1d7be165b3962986de18a2d23091e08
P2860
Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.