Comprehensive Mutation Scanning of LMNA in 268 Patients With Lone Atrial Fibrillation

American Journal of Cardiology

Volumn 103, Issue 10, 2009, Pages 1426-1428

  Brauch, Katharine M ^a   Chen, Lin Y ^c   Olson, Timothy M ^a,b  

^a MAYO CLINIC   (United States)

^b Department of Health Sciences Research   (United States)

^c NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

LAMIN A; LAMIN C;

ADULT; ARTICLE; CONGESTIVE CARDIOMYOPATHY; DISEASE ASSOCIATION; FEMALE; GENE; GENE MUTATION; GENETIC SUSCEPTIBILITY; HEART ATRIUM FIBRILLATION; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; LMNA GENE; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

ADULT; ATRIAL FIBRILLATION; CARDIOMYOPATHY, DILATED; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; LAMIN TYPE A; MALE; MIDDLE AGED; MUTATION; POLYMERASE CHAIN REACTION; SYNDROME;

EID: 65449138689     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjcard.2009.01.354     Document Type: Article

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