Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation
Author:
Funder
FWO postdoctoral grant
European Research Council
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference29 articles.
1. Clinical features of isolated ventricular noncompaction in adults long-term clinical course, echocardiographic properties, and predictors of left ventricular failure;Aras;J. Card. Fail.,2006
2. Left ventricular noncompaction: a distinct cardiomyopathy or a trait shared by different cardiac diseases?;Arbustini;JACC J. Am. Coll. Cardiol.,2014
3. Ebstein's anomaly;Attenhofer Jost;Circulation,2007
4. A novel alpha cardiac actin (ACTC1) mutation mapping to a domain in close contact with myosin heavy chain leads to a variety of congenital heart defects, arrhythmia and possibly midline defects;Augière;PLoS One,2015
5. Loss of function mutations in NNT are associated with left ventricular noncompaction;Bainbridge;Circ. Cardiovasc. Genet.,2015
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2. Altered contractility, Ca2+ transients, and cell morphology seen in a patient-specific iPSC-CM model of Ebstein’s anomaly with left ventricular noncompaction;American Journal of Physiology-Heart and Circulatory Physiology;2023-07-01
3. Nucleotide sequence variant of the TPM1 gene in a family with different phenotypes of left ventricular non-compaction;Cardiovascular Therapy and Prevention;2023-01-18
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