IndraLab

Statements

SCN4A activates SUB. 1 / 1

| 1

reach

"Both dominant and recessive forms of myotonia congenita are caused by mutations in the CLCN1 gene XREF_BIBR whilst both PMC and SCM are caused by mutations in the SCN4A gene XREF_BIBR."

23810313

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

SCN4A activates SUB. 1 / 1

INDRA sources:

Databases

Reading