IndraLab

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FGF13 binds SCN1A. 1 / 3

1 | 1

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"To further interrogate the interaction between FHF2 isoforms and Nav1.1, we also examined another mutation in Nav1.1, P1894L, which is associated with epilepsy and mild intellectual disability [ xref ]."

39996763

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IndraLab

Statements

FGF13 binds SCN1A. 1 / 3

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