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Q58798982-FF0670C3-3254-4944-B531-BD3CF84FD779
Q58798982-FF0670C3-3254-4944-B531-BD3CF84FD779
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-FF0670C3-3254-4944-B531-BD3CF84FD779
A Loss-of-Function Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
P2860
Q58798982-FF0670C3-3254-4944-B531-BD3CF84FD779
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-FF0670C3-3254-4944-B531-BD3CF84FD779
rank
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Statement
wasDerivedFrom
148c16f4ed97e3de3a34dcec95ada52e6eee2772
P2860
Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels