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Q58798982-27A3923D-381A-41B4-8741-6347011B3CF2
Q58798982-27A3923D-381A-41B4-8741-6347011B3CF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-27A3923D-381A-41B4-8741-6347011B3CF2
A Loss-of-Function Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
P921
Q58798982-27A3923D-381A-41B4-8741-6347011B3CF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-27A3923D-381A-41B4-8741-6347011B3CF2
rank
NormalRank
type
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Statement
P921
molecular biology