CELSR3 risk_factor_for TD

Subject: CELSR3
Relation: risk_factor_for
Object: TD
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017) PMID:28472652 cited

CELSR3 is a probable TD (pTD) risk gene (q < 0.3).

confidence: 0.94