NRXN1 risk_factor_for TS
Evidence from:
primary |
all sources
Evidence (1 sources)
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.
(2019)
PMID:30818990
primary
variants in known Tourette risk genes (e.g., ..., NRXN1, ...) account for fewer than 2% of affected individuals
confidence: 0.95