Novel point mutation in the NKX2-5 gene in a Moroccan...

Cardiology in the Young 2007 / 2 Vol. 17; Iss. 1

Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa

Rifai, Laïla, Maazouzi, Wajih, Sefiani, Abdelaziz
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Volume:
17
Language:
english
Journal:
Cardiology in the Young
DOI:
10.1017/s1047951106001338
Date:
February, 2007
File:
PDF, 92 KB
english, 2007
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