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Q58798982-19426132-D3D3-44D5-912A-509E68E62FC9
Q58798982-19426132-D3D3-44D5-912A-509E68E62FC9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-19426132-D3D3-44D5-912A-509E68E62FC9
A Loss-of-Function Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
P2860
Q58798982-19426132-D3D3-44D5-912A-509E68E62FC9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-19426132-D3D3-44D5-912A-509E68E62FC9
rank
NormalRank
type
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Statement
wasDerivedFrom
148c16f4ed97e3de3a34dcec95ada52e6eee2772
P2860
Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy.