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Q24679655-934CB77A-4738-4D8D-A856-A342A54900E6
Q24679655-934CB77A-4738-4D8D-A856-A342A54900E6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24679655-934CB77A-4738-4D8D-A856-A342A54900E6
A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity
P2860
Q24679655-934CB77A-4738-4D8D-A856-A342A54900E6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24679655-934CB77A-4738-4D8D-A856-A342A54900E6
rank
NormalRank
type
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Statement
wasDerivedFrom
f15356cd5c38d205382700e9942b2582db08a045
P2860
An SCN9A channelopathy causes congenital inability to experience pain