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Q37359854-4DC8EE46-0AD7-4055-AFFD-6A46330F3A22
Q37359854-4DC8EE46-0AD7-4055-AFFD-6A46330F3A22
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37359854-4DC8EE46-0AD7-4055-AFFD-6A46330F3A22
A functional null mutation of SCN1B in a patient with Dravet syndrome.
P2860
Q37359854-4DC8EE46-0AD7-4055-AFFD-6A46330F3A22
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37359854-4DC8EE46-0AD7-4055-AFFD-6A46330F3A22
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wasDerivedFrom
a8c0beff183b2f79612bd95ced4af1f2a6187040
P2860
Cargos and genes: insights into vesicular transport from inherited human disease