Found: 33
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KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.
- Published in:
- 2022
- By:
- Publication type:
- journal article
PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.
- Published in:
- 2021
- By:
- Publication type:
- journal article
ISL1 loss-of-function mutation contributes to congenital heart defects.
- Published in:
- Heart & Vessels, 2019, v. 34, n. 4, p. 658, doi. 10.1007/s00380-018-1289-z
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- Publication type:
- Article
ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.
- Published in:
- Heart & Vessels, 2018, v. 33, n. 7, p. 722, doi. 10.1007/s00380-017-1110-4
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- Publication type:
- Article
HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 7, p. 1161, doi. 10.1515/cclm-2015-0766
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- Publication type:
- Article
Prevalence and Spectrum of PITX2c Mutations Associated with Congenital Heart Disease.
- Published in:
- DNA & Cell Biology, 2013, v. 32, n. 12, p. 708, doi. 10.1089/dna.2013.2185
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- Publication type:
- Article
Discovery and functional investigation of BMP4 as a new causative gene for human congenital heart disease.
- Published in:
- American Journal of Translational Research, 2024, v. 16, n. 5, p. 2034, doi. 10.62347/DGCD4269
- By:
- Publication type:
- Article
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0124409
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- Publication type:
- Article
Association between the receptor for advanced glycation end products gene polymorphisms and coronary artery disease.
- Published in:
- Molecular Biology Reports, 2013, v. 40, n. 11, p. 6097, doi. 10.1007/s11033-013-2721-1
- By:
- Publication type:
- Article
A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.
- Published in:
- Pediatric Cardiology, 2015, v. 36, n. 7, p. 1400, doi. 10.1007/s00246-015-1173-x
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- Publication type:
- Article
A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect.
- Published in:
- Pediatric Cardiology, 2015, v. 36, n. 3, p. 646, doi. 10.1007/s00246-014-1060-x
- By:
- Publication type:
- Article
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
- Published in:
- G3: Genes | Genomes | Genetics, 2016, v. 6, n. 4, p. 987, doi. 10.1534/g3.115.026518
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- Publication type:
- Article
MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.
- Published in:
- Molecular Medicine Reports, 2017, v. 16, n. 3, p. 2747, doi. 10.3892/mmr.2017.6875
- By:
- Publication type:
- Article
Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block.
- Published in:
- Molecular Medicine Reports, 2017, v. 15, n. 4, p. 2247, doi. 10.3892/mmr.2017.6249
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- Publication type:
- Article
A novel TBX20 loss-of-function mutation contributes to adult-onset dilated cardiomyopathy or congenital atrial septal defect.
- Published in:
- Molecular Medicine Reports, 2016, v. 14, n. 4, p. 3307, doi. 10.3892/mmr.2016.5609
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- Publication type:
- Article
TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.
- Published in:
- Molecular Medicine Reports, 2016, v. 13, n. 5, p. 4349, doi. 10.3892/mmr.2016.5043
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- Publication type:
- Article
Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy.
- Published in:
- Molecular Medicine Reports, 2015, v. 12, n. 3, p. 3718, doi. 10.3892/mmr.2015.3843
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- Publication type:
- Article
Impact of prior permanent pacemaker on long-term clinical outcomes of patients undergoing percutaneous coronary intervention.
- Published in:
- Clinical Cardiology, 2017, v. 40, n. 4, p. 205, doi. 10.1002/clc.22645
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- Publication type:
- Article
Discovery of TBX20 as a Novel Gene Underlying Atrial Fibrillation.
- Published in:
- Biology (2079-7737), 2023, v. 12, n. 9, p. 1186, doi. 10.3390/biology12091186
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- Publication type:
- Article
Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias.
- Published in:
- Biology (2079-7737), 2023, v. 12, n. 3, p. 346, doi. 10.3390/biology12030346
- By:
- Publication type:
- Article
GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot.
- Published in:
- Human Mutation, 2013, v. 34, n. 12, p. 1662, doi. 10.1002/humu.22434
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- Publication type:
- Article
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 408, doi. 10.3390/genes12030408
- By:
- Publication type:
- Article
NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve.
- Published in:
- International Journal of Molecular Medicine, 2019, v. 43, n. 4, p. 1839
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- Publication type:
- Article
HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle.
- Published in:
- International Journal of Molecular Medicine, 2017, v. 39, n. 3, p. 711, doi. 10.3892/ijmm.2017.2865
- By:
- Publication type:
- Article
TBX20 loss-of-function mutation contributes to double outlet right ventricle.
- Published in:
- International Journal of Molecular Medicine, 2015, v. 35, n. 4, p. 1058, doi. 10.3892/ijmm.2015.2077
- By:
- Publication type:
- Article
GATA5 loss-of-function mutation in familial dilated cardiomyopathy.
- Published in:
- International Journal of Molecular Medicine, 2015, v. 35, n. 3, p. 763, doi. 10.3892/ijmm.2014.2050
- By:
- Publication type:
- Article
A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.
- Published in:
- International Journal of Molecular Medicine, 2015, v. 35, n. 2, p. 478, doi. 10.3892/ijmm.2014.2029
- By:
- Publication type:
- Article
NKX2-6 mutation predisposes to familial atrial fibrillation.
- Published in:
- International Journal of Molecular Medicine, 2014, v. 34, n. 6, p. 1581, doi. 10.3892/ijmm.2014.1971
- By:
- Publication type:
- Article
GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy.
- Published in:
- International Journal of Molecular Medicine, 2014, v. 34, n. 5, p. 1315, doi. 10.3892/ijmm.2014.1896
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- Publication type:
- Article
GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.
- Published in:
- International Journal of Molecular Medicine, 2014, v. 33, n. 5, p. 1219, doi. 10.3892/ijmm.2014.1700
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- Publication type:
- Article
Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2021, v. 59, n. 5, p. 955, doi. 10.1515/cclm-2020-1318
- By:
- Publication type:
- Article
MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2018, v. 56, n. 3, p. 502, doi. 10.1515/cclm-2017-0461
- By:
- Publication type:
- Article
CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 9, p. 1417, doi. 10.1515/cclm-2016-0612
- By:
- Publication type:
- Article