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SCN1A activates FHM2. 2 / 2

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"FHM1, FHM2 and FHM3 are caused by mutations in the ion-channel genes CACNA1A, ATP1A2 and SCN1A, respectively [XREF_BIBR - XREF_BIBR]."

18846413

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"FHM is a genetically heterogeneous disease, in which mutations can occur in the ion transportation genes CACNA1A, ATP1A2, and SCN1A, promoting the different types of familial migraines, FHM1, FHM2 and FHM3."

27313535

INDRA sources:

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IndraLab

Statements

SCN1A activates FHM2. 2 / 2

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