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Q28080066-3E986F85-A00A-4C3E-8938-4A2BF6B4BDC6
Q28080066-3E986F85-A00A-4C3E-8938-4A2BF6B4BDC6
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http://www.wikidata.org/entity/statement/Q28080066-3E986F85-A00A-4C3E-8938-4A2BF6B4BDC6
Understanding Genotypes and Phenotypes in Epileptic Encephalopathies
P2860
Q28080066-3E986F85-A00A-4C3E-8938-4A2BF6B4BDC6
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http://www.wikidata.org/entity/statement/Q28080066-3E986F85-A00A-4C3E-8938-4A2BF6B4BDC6
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4194f77e56faa33201a3ecaeb63f1dcf3c9bd5c3
P2860
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome