IndraLab

Statements

Mutated SCN4A activates phenotype. 1 / 1

| 1

reach

"This phenotype, also named NormoPP, is caused by SCN4A mutations at deeper locations of the voltage sensor of domain II at codon 675."

20237798

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 SCN4A activates phenotype. 1 / 1

INDRA sources:

Databases

Reading