Found: 6
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Lamin-A/C variants found in patients with cardiac conduction disease reduce sodium currents.
- Published in:
- Cardiogenetics, 2018, v. 8, n. 1, p. 4, doi. 10.4081/cardiogenetics.2018.7127
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- Publication type:
- Article
A post mortem assessment of a 25-year-old man with ascending aortic dissection and a novel MYLK variant.
- Published in:
- Cardiogenetics, 2015, v. 5, n. 1, p. 13, doi. 10.4081/cardiogenetics.2015.5251
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- Publication type:
- Article
Intragenic CFTR Duplication and 5T/12TG Variant in a Patient with Non-Classic Cystic Fibrosis.
- Published in:
- Scientific Reports, 2016, p. 38776, doi. 10.1038/srep38776
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- Publication type:
- Article
MIB2 variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathy.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 1, p. 33, doi. 10.1093/hmg/ddw365
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- Publication type:
- Article
Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel.
- Published in:
- 2016
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- Publication type:
- Correction Notice
Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel.
- Published in:
- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0143588
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- Publication type:
- Article