IndraLab

Statements

Mutated KCNQ1 activates Arg-Trp. 1 / 1

| 1

reach

"Heterozygous KCNQ1 mutations cause the dominant RW LQT1 syndrome and is the most common LQTS genotype accounting for 30-35% of LQTS."

23684683

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

Mutated KCNQ1 activates Arg-Trp. 1 / 1

INDRA sources:

Databases

Reading