Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction
Background Ebstein's anomaly (EA) is a rare congenital heart disease of the tricuspid valve and right ventricle. Patients with EA often manifest with left ventricular noncompaction (LVNC), a cardiomyopathy. Despite implication of cardiac sarcomere genes in some cases, very little is understood...
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| Published in: | Molecular genetics & genomic medicine Vol. 8; no. 4; pp. e1152 - n/a |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
John Wiley & Sons, Inc
01.04.2020
John Wiley and Sons Inc Wiley |
| Subjects: | |
| ISSN: | 2324-9269, 2324-9269 |
| Online Access: | Get full text |
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