Parent, John J.Towbin, Jeffrey A.Jefferies, John L.2016-06-152016-06-152015-02Parent, 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-13-38431526-6702https://hdl.handle.net/1805/9990Left 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-USPublisher PolicyIsolated Noncompaction of the Ventricular MyocardiumGeneticsLamin Type AMutationLeft ventricular noncompaction in a family with lamin A/C gene mutationArticle