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Q36139482-C65A0BED-424F-48C8-BEA2-356CD775357E
Q36139482-C65A0BED-424F-48C8-BEA2-356CD775357E
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http://www.wikidata.org/entity/statement/Q36139482-C65A0BED-424F-48C8-BEA2-356CD775357E
The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited Erythromelalgia.
P2860
Q36139482-C65A0BED-424F-48C8-BEA2-356CD775357E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36139482-C65A0BED-424F-48C8-BEA2-356CD775357E
rank
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type
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wasDerivedFrom
4b26fff546b17eee703bc67a30e38d0df2930761
P2860
Inherited pain: sodium channel Nav1.7 A1632T mutation causes erythromelalgia due to a shift of fast inactivation.