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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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- Article
Plasma ghrelin levels are closely associated with severity and morphology of angiographically-detected coronary atherosclerosis in Chineses patients with diabetes mellitus.
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- Acta Pharmacologica Sinica, 2012, v. 33, n. 4, p. 452, doi. 10.1038/aps.2011.196
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- Article
Prevalence and Spectrum of PITX2c Mutations Associated with Congenital Heart Disease.
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- DNA & Cell Biology, 2013, v. 32, n. 12, p. 708, doi. 10.1089/dna.2013.2185
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- Article
A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect.
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- Pediatric Cardiology, 2015, v. 36, n. 3, p. 646, doi. 10.1007/s00246-014-1060-x
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- Article
Impact of prior permanent pacemaker on long-term clinical outcomes of patients undergoing percutaneous coronary intervention.
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- Clinical Cardiology, 2017, v. 40, n. 4, p. 205, doi. 10.1002/clc.22645
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- Article
GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot.
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- Human Mutation, 2013, v. 34, n. 12, p. 1662, doi. 10.1002/humu.22434
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- Article
MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
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- Clinical Chemistry & Laboratory Medicine, 2018, v. 56, n. 3, p. 502, doi. 10.1515/cclm-2017-0461
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- Article