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Q39457643-F661E585-6C89-4A91-AD86-BA13DED08379
Q39457643-F661E585-6C89-4A91-AD86-BA13DED08379
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39457643-F661E585-6C89-4A91-AD86-BA13DED08379
Models for discovery of targeted therapy in genetic epileptic encephalopathies.
P2860
Q39457643-F661E585-6C89-4A91-AD86-BA13DED08379
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39457643-F661E585-6C89-4A91-AD86-BA13DED08379
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wasDerivedFrom
e81ed1a6beae3786b947e61fa7b18636a7e3e2f2
P2860
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome