Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects
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Of mice and men: molecular genetics of congenital heart diseaseA Murine Myh6MerCreMer Knock-In Allele Specifically Mediates Temporal Genetic Deletion in Cardiomyocytes after Tamoxifen InductionChamber Specific Gene Expression Landscape of the Zebrafish HeartExome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrestPossible Biomarkers for the Early Detection of HIV-associated Heart Diseases: A Proteomics and Bioinformatics PredictionMolecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencingA systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field.Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.DNA Microarray Analysis in Screening Features of Genes Involved in Spinal Cord Injury.Critical roles for multiple formins during cardiac myofibril development and repair.Heavy and light roles: myosin in the morphogenesis of the heart.Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.Impact of MYH6 variants in hypoplastic left heart syndrome.Advances in molecular genetics for pulmonary atresia.Integrated Transcriptome Map Highlights Structural and Functional Aspects of the Normal Human HeartParental occupational exposures to endocrine disruptors and the risk of simple isolated congenital heart defects.Formation, contraction, and mechanotransduction of myofribrils in cardiac development: clues from genetics.Familial co-occurrence of congenital heart defects follows distinct patterns.Experience with genomic sequencing in pediatric patients with congenital cardiac defects in a large community hospital.A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES).CCN1 mutation is associated with atrial septal defect.Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease.Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval
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P2860
Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects
description
2011 nî lūn-bûn
@nan
2011 թուականին հրատարակուած գիտական յօդուած
@hyw
2011 թվականին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@ast
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@en
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@en-gb
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@nl
type
label
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@ast
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@en
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@en-gb
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@nl
prefLabel
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@ast
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@en
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@en-gb
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@nl
P2093
P2860
P50
P3181
P1433
P1476
Cardiac alpha-myosin (MYH6) is ...... familial atrial septal defects
@en
P2093
Bernard De Geeter
Cemil Özcelik
Claire Dauphin
Dany Yousseff
David Fournier
Katharina R Schmitt
Maximilian G Posch
Melanie Müller
Miguel A Andrade-Navarro
Patrice Bouvagnet
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0028872
P407
P577
2011-12-14T00:00:00Z