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Q35696704-867A239A-E31B-46E5-B51C-57CF253CBB64
Q35696704-867A239A-E31B-46E5-B51C-57CF253CBB64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35696704-867A239A-E31B-46E5-B51C-57CF253CBB64
First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy
P2860
Q35696704-867A239A-E31B-46E5-B51C-57CF253CBB64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35696704-867A239A-E31B-46E5-B51C-57CF253CBB64
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
b726c0e1416048f65ba0fdeec055e014a733a453
P2860
Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels