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Q37359854-1EA2CA3E-E3A5-41A0-B0F6-5C700F3AB1AD
Q37359854-1EA2CA3E-E3A5-41A0-B0F6-5C700F3AB1AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37359854-1EA2CA3E-E3A5-41A0-B0F6-5C700F3AB1AD
A functional null mutation of SCN1B in a patient with Dravet syndrome.
P2860
Q37359854-1EA2CA3E-E3A5-41A0-B0F6-5C700F3AB1AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37359854-1EA2CA3E-E3A5-41A0-B0F6-5C700F3AB1AD
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Statement
wasDerivedFrom
a8c0beff183b2f79612bd95ced4af1f2a6187040
P2860
Epileptogenic channelopathies: experimental models of human pathologies.