Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction.

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Abstract

Left ventricular noncompaction (LVNC) is an autosomal-dominant, genetically heterogeneous cardiomyopathy with variable severity, which may co-occur with cardiac hypertrophy.

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Journal

Journal ID (iso-abbrev): Circ Cardiovasc Genet

Title: Circulation. Cardiovascular genetics

Publisher: Ovid Technologies (Wolters Kluwer Health)

ISSN (Electronic): 1942-3268

ISSN (Print): 1942-3268

Publication date (Electronic): Aug 2015

Volume: 8

Issue: 4

Affiliations

[1 ] From the Human Genome Sequencing Center (M.N.B., M.W., H.D., D.M., E.B., R.G.), Department Pediatrics-Cardiology, Baylor College of Medicine, Houston, TX (H.R.M., R.P., J.L.J.); Codified Genomics, LLC, Houston, TX (M.N.B.); Center for Human Disease Modeling, Duke University Medical Center, Durham, NC (E.E.D., N.K.); and Department of Cell Biology, Duke University, Durham, NC (W.-Y.C., A.D.).

[2 ] From the Human Genome Sequencing Center (M.N.B., M.W., H.D., D.M., E.B., R.G.), Department Pediatrics-Cardiology, Baylor College of Medicine, Houston, TX (H.R.M., R.P., J.L.J.); Codified Genomics, LLC, Houston, TX (M.N.B.); Center for Human Disease Modeling, Duke University Medical Center, Durham, NC (E.E.D., N.K.); and Department of Cell Biology, Duke University, Durham, NC (W.-Y.C., A.D.). agibbs@bcm.edu john.jefferies@cchmc.org.

Article

Publisher Item ID: CIRCGENETICS.115.001026 Mid ID: NIHMS699260

DOI: 10.1161/CIRCGENETICS.115.001026

PMC ID: 4545476

PubMed ID: 26025024

SO-VID: a65b15ec-4268-438d-a0f5-d254bc821769

History

Keywords: genetics,genomics,human,mutation,nonisolated left ventricular noncompaction

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Keywords: genetics, genomics, human, mutation, nonisolated left ventricular noncompaction

Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction.

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