IndraLab

Statements

KCNA1 activates Episodic ataxia 1. 1 / 1

| 1

reach

"Episodic ataxia 1 is caused by dominantly inherited or de novo missense or nonsense mutations in the KCNA1 gene [XREF_BIBR, XREF_BIBR, XREF_BIBR]."

26395884

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

KCNA1 activates Episodic ataxia 1. 1 / 1

INDRA sources:

Databases

Reading