Table 6 Association of DNAH11 mutations with the risk of congenital heart disease and heterotaxy syndrome.

From: DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome

Characteristic

CHD/heterotaxy casesa

(n = 45)

CHD cases

(n = 98)

P b

No. of patients with mutation

8

0

0.0001

  1. aCHD/heterotaxy: congenital heart disease/heterotaxy; bFisher’s exact test was used.
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