X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by emerin mutation

Journal of Cardiovascular Electrophysiology

Volumn 19, Issue 5, 2008, Pages 510-515

  Karst, Margaret L ^a   Herron, Kathleen J ^a   Olson, Timothy M ^a,b  

^a Department of Health Sciences Research   (United States)

^b MAYO CLINIC   (United States)

Author keywords

Atrial fibrillation; Emerin; LEM domain; Sinus node dysfunction; X linked

Indexed keywords

EMERIN; LYSINE; MEMBRANE PROTEIN; NUCLEAR PROTEIN;

ADULT; ARTICLE; CHEEK MUCOSA; CHROMOSOME XQ; CLINICAL ARTICLE; DNA DETERMINATION; DNA SEQUENCE; ELECTROCARDIOGRAPHY; EMERIN GENE; EMERY DREIFUSS MUSCULAR DYSTROPHY; EPITHELIUM CELL; FAMILIAL DISEASE; FAMILY HISTORY; GENE; GENE DELETION; GENE DISRUPTION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE TARGETING; GENEALOGY; GENOTYPE; HEART ATRIUM FIBRILLATION; HEMIZYGOSITY; HETEROZYGOSITY; HUMAN; HUMAN CELL; MALE; MEDICAL RECORD; MUSCLE CONTRACTURE; MYOPATHY; PAROXYSMAL SUPRAVENTRICULAR TACHYCARDIA; PRIORITY JOURNAL; PROSPECTIVE STUDY; PROTEIN ASSEMBLY; PROTEIN BINDING; SINUS NODE DYSFUNCTION; X CHROMOSOMAL INHERITANCE; X LINKED NONSYNDROMIC SINUS NODE DYSFUNCTION;

ADULT; ATRIAL FIBRILLATION; GENETIC DISEASES, X-LINKED; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; NUCLEAR PROTEINS; PEDIGREE; SINOATRIAL NODE;

EID: 43049129979     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/j.1540-8167.2007.01081.x     Document Type: Article

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