emerin and Stroke

emerin has been researched along with Stroke* in 1 studies

Other Studies

1 other study(ies) available for emerin and Stroke

Article	Year
Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction. Circulation. Arrhythmia and electrophysiology, 2020, Volume: 13, Issue:10 Mutations in the nuclear envelope genes encoding. Targeted exon sequencing was performed in 87 probands with familial sick sinus syndrome (n=36) and a progressive cardiac conduction defect (n=51).. We identified 3 X-linked recessive. Cardiac emerinopathy is a novel nonsyndromic X-linked progressive atrial standstill associated with LVNC and increased risk of thromboembolism. Topics: Adolescent; Adult; Aged; Cardiac Conduction System Disease; Cardiomyopathies; Child; Female; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Heart Atria; Heart Block; Humans; Isolated Noncompaction of the Ventricular Myocardium; Male; Membrane Proteins; Middle Aged; Mutation; Nuclear Proteins; Phenotype; Sick Sinus Syndrome; Stroke; Thromboembolism; X-Linked Emery-Dreifuss Muscular Dystrophy; Young Adult	2020

Article

Year

Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction.

Circulation. Arrhythmia and electrophysiology, 2020, Volume: 13, Issue:10

Mutations in the nuclear envelope genes encoding. Targeted exon sequencing was performed in 87 probands with familial sick sinus syndrome (n=36) and a progressive cardiac conduction defect (n=51).. We identified 3 X-linked recessive. Cardiac emerinopathy is a novel nonsyndromic X-linked progressive atrial standstill associated with LVNC and increased risk of thromboembolism.

Topics: Adolescent; Adult; Aged; Cardiac Conduction System Disease; Cardiomyopathies; Child; Female; Genetic Diseases, Inborn; Genetic Predisposition to Disease; Heart Atria; Heart Block; Humans; Isolated Noncompaction of the Ventricular Myocardium; Male; Membrane Proteins; Middle Aged; Mutation; Nuclear Proteins; Phenotype; Sick Sinus Syndrome; Stroke; Thromboembolism; X-Linked Emery-Dreifuss Muscular Dystrophy; Young Adult

2020