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Q34359072-3778D4F7-D779-418E-A4FA-250385364C86
Q34359072-3778D4F7-D779-418E-A4FA-250385364C86
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34359072-3778D4F7-D779-418E-A4FA-250385364C86
Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.
P2860
Q34359072-3778D4F7-D779-418E-A4FA-250385364C86
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34359072-3778D4F7-D779-418E-A4FA-250385364C86
rank
NormalRank
type
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Statement
wasDerivedFrom
39f9f0a2f72f4182fa14b77612ac616b6a072c31
P2860
Sodium channels SCN1A, SCN2A and SCN3A in familial autism