Investigation of somatic NKX2-5 mutations in congenital heart disease
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Identification of de novo mutations and rare variants in hypoplastic left heart syndromeGenetics of Congenital Heart Defects: The NKX2-5 Gene, a Key PlayerTargeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.The molecular genetics of congenital heart disease: a review of recent developments.Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysisDNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot.Transcriptional defect of an inherited NKX2-5 haplotype comprising a SNP, a nonsynonymous and a synonymous mutation, associated with human congenital heart disease.Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease.Differences in Copy Number Variation between Discordant Monozygotic Twins as a Model for Exploring Chromosomal Mosaicism in Congenital Heart Defects.An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defectsmiR-30c regulates proliferation, apoptosis and differentiation via the Shh signaling pathway in P19 cells.Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of Fallot.From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases.Congenital heart disease: the crossroads of genetics, epigenetics and environment.Hypoplastic Left Heart Syndrome Sequencing Reveals a Novel NOTCH1 Mutation in a Family with Single Ventricle Defects.The c.63A>G polymorphism in the NKX2.5 gene is associated with thyroid hypoplasia in children with thyroid dysgenesis.NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population.Novel Point Mutations in the Gene in Pediatric Patients with Non-Familial Congenital Heart Disease
P2860
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P2860
Investigation of somatic NKX2-5 mutations in congenital heart disease
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article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on February 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Investigation of somatic NKX2-5 mutations in congenital heart disease
@en
Investigation of somatic NKX2-5 mutations in congenital heart disease.
@nl
type
label
Investigation of somatic NKX2-5 mutations in congenital heart disease
@en
Investigation of somatic NKX2-5 mutations in congenital heart disease.
@nl
prefLabel
Investigation of somatic NKX2-5 mutations in congenital heart disease
@en
Investigation of somatic NKX2-5 mutations in congenital heart disease.
@nl
P2093
P2860
P356
P1476
Investigation of somatic NKX2-5 mutations in congenital heart disease
@en
P2093
A Tomita-Mitchell
E H Austin
M E Mitchell
P2860
P304
P356
10.1136/JMG.2008.060277
P407
P577
2009-02-01T00:00:00Z