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Q41669692-3D02E4B2-ABF8-496C-92E4-B2A1E746FB29
Q41669692-3D02E4B2-ABF8-496C-92E4-B2A1E746FB29
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41669692-3D02E4B2-ABF8-496C-92E4-B2A1E746FB29
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.
P2860
Q41669692-3D02E4B2-ABF8-496C-92E4-B2A1E746FB29
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41669692-3D02E4B2-ABF8-496C-92E4-B2A1E746FB29
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type
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Statement
wasDerivedFrom
b1edee0b38d19ef66d82b175fc48c588a961fbcf
P2860
Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.