Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype
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The Current Approach to Diagnosis and Management of Left Ventricular Noncompaction Cardiomyopathy: Review of the LiteratureLoss of Function Mutations in NNT Are Associated With Left Ventricular NoncompactionGenetics and disease of ventricular muscle.Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defectsDigenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathyHeart failure in patients with normal coronary anatomy: diagnostic algorithm and disease pattern of various etiologies as defined by cardiac MRI.A novel ACTC1 mutation in a young boy with left ventricular noncompaction and arrhythmias.MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques.Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies.Almanac 2011: cardiomyopathies. The national society journals present selected research that has driven recent advances in clinical cardiology.The pathogenicity of genetic variants previously associated with left ventricular non-compaction.Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.Molecular mechanism of ventricular trabeculation/compaction and the pathogenesis of the left ventricular noncompaction cardiomyopathy (LVNC)Implications of genetic testing in noncompaction/hypertrabeculation.Interpreting secondary cardiac disease variants in an exome cohort.Isolated left ventricular noncompaction: what do we really know?16-kDa prolactin and bromocriptine in postpartum cardiomyopathy.A study of tropomyosin's role in cardiac function and disease using thin-filament reconstituted myocardium.Alpha-tropomyosin mutations in inherited cardiomyopathies.A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.Genetic Testing Is Not Required for Diagnosing Left Ventricular Hypertrabeculation / Non-Compaction.Acquired non-compaction in integrin-myopathyA low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction.Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy.Inherited cardiomyopathies and sports participation.Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience
P2860
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P2860
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype
description
2011 nî lūn-bûn
@nan
2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին 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
Sarcomere gene mutations in is ...... not predict clinical phenotype
@ast
Sarcomere gene mutations in is ...... not predict clinical phenotype
@en
Sarcomere gene mutations in is ...... not predict clinical phenotype
@nl
type
label
Sarcomere gene mutations in is ...... not predict clinical phenotype
@ast
Sarcomere gene mutations in is ...... not predict clinical phenotype
@en
Sarcomere gene mutations in is ...... not predict clinical phenotype
@nl
prefLabel
Sarcomere gene mutations in is ...... not predict clinical phenotype
@ast
Sarcomere gene mutations in is ...... not predict clinical phenotype
@en
Sarcomere gene mutations in is ...... not predict clinical phenotype
@nl
P2093
P3181
P1476
Sarcomere gene mutations in is ...... not predict clinical phenotype
@en
P2093
Erwin Oechslin
Ludwig Thierfelder
Matthias Greutmann
Philipp Boyé
Pia Schuler
Sabine Klaassen
Susanne Probst
Walter Knirsch
P304
P3181
P356
10.1161/CIRCGENETICS.110.959270
P407
P577
2011-08-01T00:00:00Z