Familial accumulation of sudden cardiac deaths and the LMNA variant c.868G>A (p.Glu290Lys)
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference24 articles.
1. First Japanese case of atypical progeroid syndrome/atypical Werner syndrome with heterozygous LMNA mutation;Motegi;J. Dermatol.,2014
2. A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement;Hattori;Neuromuscul. Disord.,2012
3. A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene;Ambrosi;Int. J. Cardiol.,2016
4. A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death;Pérez-Serra;J. Card. Fail.,2015
5. Expanding the phenotype of sudden cardiac death — an unusual presentation of a family with a Lamin A/C mutation;De Backer;Int. J. Cardiol.,2010
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