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Association of DNAH11 mutations with the risk of 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 |
aCHD/heterotaxy: congenital heart disease/heterotaxy; bFisher’s exact test was used.
