Left ventricular noncompaction in a family with lamin A/C gene mutation

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dc.contributor.authorParent, John J.
dc.contributor.authorTowbin, Jeffrey A.
dc.contributor.authorJefferies, John L.
dc.contributor.departmentDepartment of Pediatrics, IU School of Medicineen_US
dc.date.accessioned2016-06-15T21:15:12Z
dc.date.available2016-06-15T21:15:12Z
dc.date.issued2015-02
dc.description.abstractLeft ventricular noncompaction is a rare type of cardiomyopathy, the genetics of which are poorly understood to date. Lamin A/C gene mutations have been associated with dilated cardiomyopathy and diseases of the conduction system, but rarely in left ventricular noncompaction cardiomyopathy. This report describes the cases of 4 family members with a lamin A/C gene mutation, 3 of whom had phenotypic expression of left ventricular noncompaction.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationParent, J. J., Towbin, J. A., & Jefferies, J. L. (2015). Left Ventricular Noncompaction in a Family with Lamin A/C Gene Mutation. Texas Heart Institute Journal, 42(1), 73–76. http://doi.org/10.14503/THIJ-13-3843en_US
dc.identifier.issn1526-6702en_US
dc.identifier.urihttps://hdl.handle.net/1805/9990
dc.language.isoen_USen_US
dc.publisherTexas Heart Institute Journalen_US
dc.relation.isversionof10.14503/THIJ-13-3843en_US
dc.relation.journalTexas Heart Institute Journalen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectIsolated Noncompaction of the Ventricular Myocardiumen_US
dc.subjectGeneticsen_US
dc.subjectLamin Type Aen_US
dc.subjectMutationen_US
dc.titleLeft ventricular noncompaction in a family with lamin A/C gene mutationen_US
dc.typeArticleen_US
ul.alternative.fulltexthttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378052/en_US
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