IndraLab

Statements

KCNQ1 activates GHD. 1 / 1

| 1

reach

"We identified two missense mutations in KCNQ1 to underlie childhood onset of GHD and maternally inherited gingival fibromatosis."

29097701

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 GHD. 1 / 1

INDRA sources:

Databases

Reading