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Q58798982-72A6DDDB-7F14-4A15-A373-B3D08F1EDC92
Q58798982-72A6DDDB-7F14-4A15-A373-B3D08F1EDC92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-72A6DDDB-7F14-4A15-A373-B3D08F1EDC92
A Loss-of-Function Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
P2860
Q58798982-72A6DDDB-7F14-4A15-A373-B3D08F1EDC92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-72A6DDDB-7F14-4A15-A373-B3D08F1EDC92
rank
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type
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Statement
wasDerivedFrom
148c16f4ed97e3de3a34dcec95ada52e6eee2772
P2860
Absence epilepsy in apathetic, a spontaneous mutant mouse lacking the h channel subunit, HCN2