IndraLab

Statements

SCN1A activates ATP1A2. 1 / 1

| 1

reach

"On the other hand, FHM2 and FHM3, caused by mutations of the ATP1A2 gene and SCN1A gene, respectively [13], have not been widely associated with sole MO, corresponding to the theory regarding their different pathophysiology."

40229683

INDRA sources:

Colored badges next to statement headings correspond to evidence counts from knowledge sources, as shown below. Badges to the left of the | separator correspond to curated knowledge base sources, and badges to the right of it correspond to machine reading systems.

IndraLab

Statements

SCN1A activates ATP1A2. 1 / 1

INDRA sources:

Databases

Reading