The association between FOXP2 (Forkhead Box P2) and Childhood Apraxia Of Speech is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants161
Symptoms28
Compounds0
Trials0
Publications16
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.