CLTCL1 associated_with intellectual disability

Subject: CLTCL1
Relation: associated_with
Object: intellectual disability
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012) PMID:22511880 cited

CLTCL1 is disrupted in a patient with features of DiGeorge syndrome, including intellectual disability.

confidence: 0.85