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Paper Details

Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1.
Circ Res
4
2023
ADAM metallopeptidase, ADAMTS1, CHD4, CHD4 protein, ECM, Human, Human CHD4, LVNC, Left ventricular noncompaction, Patients, SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily, Ventricular Noncompaction, biventricular hypertrabeculation, cardiac defects, cardiac dysfunction, cardiac genes, cardiomyocytes, cardiomyopathy, chromatin, chromodomain helicase DNA-binding protein 4, congenital heart defects, endocardial BRG1, human, humanized, humans, hyperproliferation, hypertrabeculation defects, mice, mouse, mouse CHD4, mutation, mutation CHD4, noncompaction, sudden death, thrombospondin type 1 motif 1, ventricular wall defects
Author NameAffiliation
Christine E SeidmanHarvard Medical School
Christine E SeidmanBrigham and Women's Hospital
Christine E SeidmanHoward Hughes Medical Institute
Christine E SeidmanHarvard Medical School
Christine E SeidmanHoward Hughes Medical Institute
Christine E SeidmanBrigham and Women's Hospital
Jonathan G Seidmanthe University of North Carolina at Chapel Hill.
Jonathan G SeidmanHarvard Medical School
Jonathan G Seidmanthe University of North Carolina at Chapel Hill.
Jonathan G SeidmanHarvard Medical School
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