IndraLab

Statements

SCN1A activates FHM. 3 / 3
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"So far, mutations in three different genes, CACNA1A, ATP1A2, and SCN1A, have been described to cause FHM and they are referred as FHM1, FHM2, and FHM3, respectively."
29867740
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"Gene mutations of CACNA1A, SCN1A, and ATP1A2 can cause FHM and we investigated only CACNA1A gene mutation in the present case that revealed negative result."
28101483
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"XREF_BIBR Rare mutations in the CACNA1A, ATP1A2 and SCN1A genes can all cause FHM, revealing genetic heterogeneity in the disorder."
31980564