Novel NKX2-5 mutations in patients with familial atrial septal defects.
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Genetics of Congenital Heart Defects: The NKX2-5 Gene, a Key PlayerPreconceptual Folic Acid Use and Recurrence Risk Counseling for Congenital Heart Disease.Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillationMouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation.A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.The HAND1 frameshift A126FS mutation does not cause hypoplastic left heart syndrome in mice.NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population.Risk of congenital heart disease in relatives of probands with conotruncal cardiac defects: an evaluation of 1,620 families.
P2860
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P2860
Novel NKX2-5 mutations in patients with familial atrial septal defects.
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2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年學術文章
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name
Novel NKX2-5 mutations in patients with familial atrial septal defects.
@en
Novel NKX2-5 mutations in patients with familial atrial septal defects.
@nl
type
label
Novel NKX2-5 mutations in patients with familial atrial septal defects.
@en
Novel NKX2-5 mutations in patients with familial atrial septal defects.
@nl
prefLabel
Novel NKX2-5 mutations in patients with familial atrial septal defects.
@en
Novel NKX2-5 mutations in patients with familial atrial septal defects.
@nl
P2093
P2860
P1433
P1476
Novel NKX2-5 mutations in patients with familial atrial septal defects.
@en
P2093
Jing-Hao Zheng
Xiao-Zhong Chen
Xiao-Zhou Wang
Xing-Yuan Liu
Yang-Yang Zhang
Yi-Han Chen
Yi-Qing Yang
P2860
P2888
P304
P356
10.1007/S00246-010-9859-6
P577
2010-12-25T00:00:00Z