NKX2.5mutations in patients with congenital heart disease
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference25 articles.
1. Congenital heart disease caused by mutations in the transcription factor NKX2-5;Schott;Science,1998
2. Mutations in the cardiac transcription factor NKX2.5affect diverse cardiac developmental pathways;Benson;J Clin Invest,1999
3. Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient;Hosoda;Jpn Circ J,1999
4. NKX2.5mutations in patients with tetralogy of Fallot;Goldmuntz;Circulation,2001
5. Frequency of 22q11 deletions in patients with conotruncal defects;Goldmuntz;J Am Coll Cardiol,1998
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