IndraLab

Statements

SCN1A binds CACNA1A, ATP1A2, and ATP1A2. 1 / 1

| 1

sparser

"Mutations in CACNA1A, ATP1A2 and SCN1A genes have been associated with familial hemiplegic migraine (FHM), a rare monogenic form of migraine [ xref ]."

23566281

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 binds CACNA1A, ATP1A2, and ATP1A2. 1 / 1

INDRA sources:

Databases

Reading