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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Bibliographic Details
Published in:Molecular genetics & genomic medicine Vol. 8; no. 4; pp. e1152 - n/a
Main Authors: Samudrala, Sai Suma K., North, Lauren M., Stamm, Karl D., Earing, Michael G., Frommelt, Michele A., Willes, Richard, Tripathi, Swarnendu, Dsouza, Nikita R., Zimmermann, Michael T., Mahnke, Donna K., Liang, Huan Ling, Lund, Michael, Lin, Chien‐Wei, Geddes, Gabrielle C., Mitchell, Michael E., Tomita‐Mitchell, Aoy
Format: Journal Article
Language:English
Published: United States John Wiley & Sons, Inc 01.04.2020
John Wiley and Sons Inc
Wiley
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ISSN:2324-9269, 2324-9269
Online Access:Get full text
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