IndraLab

Statements

SCN9A activates PE. 1 / 1

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"PE is exclusively caused by mutations in SCN9A, the encoding gene of sodium channel subtype Nav1.7 and can be sub-classified into familial (inherited erythromelalgia) and sporadic forms."

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INDRA sources:

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IndraLab

Statements

SCN9A activates PE. 1 / 1

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