The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes
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Title
The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes
Authors
Keywords
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Journal
Diagnostics
Volume 12, Issue 5, Pages 1132
Publisher
MDPI AG
Online
2022-05-03
DOI
10.3390/diagnostics12051132
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Related references
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- Yield of Rare Variants Detected by Targeted Next-Generation Sequencing in a Cohort of Romanian Index Patients with Hypertrophic Cardiomyopathy
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- Y-chromosomal connection between Hungarians and geographically distant populations of the Ural Mountain region and West Siberia
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- Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy
- (2018) Richard D. Bagnall et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy
- (2018) Juan Pablo Ochoa et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes
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- Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy
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- Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing
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- 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
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- Characterization of a Phenotype-Based Genetic Test Prediction Score for Unrelated Patients With Hypertrophic Cardiomyopathy
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- Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing
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- Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population
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- Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands
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