From: A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder
Number of subjects
Exonic deletions
Exonic deletion frequency (%)
P valuea
Frameshift deletions
Frameshift deletion frequency (%)
ASD cases
2,147
16b
0.37
0.62
6b
0.14
0.56
Controls
6,639
43
0.32
14
0.11