Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
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Importance of genetic evaluation and testing in pediatric cardiomyopathyStructure of the large ribosomal subunit from human mitochondria.Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA.Mitochondrial DNA Sequence Variation Associated With Peripheral Nerve Function in the Elderly.MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family.Tafazzin knockdown in mice leads to a developmental cardiomyopathy with early diastolic dysfunction preceding myocardial noncompaction.Next generation sequencing to characterize mitochondrial genomic DNA heteroplasmy.Mitochondrial Respiratory Defect Causes Dysfunctional Lactate Turnover via AMP-activated Protein Kinase Activation in Human-induced Pluripotent Stem Cell-derived Hepatocytes.Challenges of bringing next generation sequencing technologies to clinical molecular diagnostic laboratoriesNoncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C diseaseA novel association of biventricular cardiac noncompaction and diabetic embryopathy: case report and review of the literature.Mitochondrial Heteroplasmy.Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.Genetic Testing Is Not Required for Diagnosing Left Ventricular Hypertrabeculation / Non-Compaction.Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects.Association of low race performance with mtDNA haplogroup L3b of Australian thoroughbred horses.Transition m.3308T>C in the ND1 gene is associated with left ventricular hypertrabeculation/noncompaction.Mitochondrial mutations in patients with congenital heart defects by next generation sequencing technology.Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.Isolation and analysis of genes mainly expressed in adult mouse heart using subtractive hybridization cDNA library.ATP Synthase Diseases of Mitochondrial Genetic Origin.Decreased glycolytic metabolism in non-compaction cardiomyopathy by 18F-fluoro-2-deoxyglucose positron emission tomography: new insights into pathophysiological mechanisms and clinical implications
P2860
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P2860
Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
description
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
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
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2010年學術文章
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name
Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
@en
Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
@nl
type
label
Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
@en
Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
@nl
prefLabel
Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
@en
Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
@nl
P2093
P1433
P1476
Left ventricular noncompaction is associated with mutations in the mitochondrial genome
@en
P2093
Anjan Batra
Eric S Ebenroth
P304
P356
10.1016/J.MITO.2010.02.003
P50
P577
2010-03-06T00:00:00Z