IndraLab

Statements

ID1 binds KCNA2. 1 / 1

| 1

sparser

"Recently, de novo KCNA2 missense mutations were associated with epileptic encephalopathy, ataxia, variable ID xref , xref and other features reminiscent of those found in family PKMR82."

27457812

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

ID1 binds KCNA2. 1 / 1

INDRA sources:

Databases

Reading