IndraLab

Statements

KCNQ1 activates SQTL1. 1 / 1

| 1

reach

"173 The most common mutation occurs in the KCNQ1 gene, which is responsible for more than 30% of the genetic variants and pathological mutations identified in LQTS and causes SQTL1."

30916199

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

KCNQ1 activates SQTL1. 1 / 1

INDRA sources:

Databases

Reading