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Table 1 Frequency of CTNNA3 exonic deletions in ASD cases and controls

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 (%)

P valuea

ASD cases

2,147

16b

0.37

0.62

6b

0.14

0.56

Controls

6,639

43

0.32

 

14

0.11

 
  1. aFisher's exact test; bIncluding the two exon 11 deletions in family 3456.
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Journal of Neurodevelopmental Disorders

ISSN: 1866-1955

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