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Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene
Bjørnstad, Per G., Leren, Trond P.Volume:
19
Language:
english
Journal:
Cardiology in the Young
DOI:
10.1017/s1047951108003387
Date:
February, 2009
File:
PDF, 173 KB
english, 2009