CorrespondenceFamilial accumulation of sudden cardiac deaths and the LMNA variant c.868G > A (p.Glu290Lys)
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Conflict of interest
The authors have nothing to declare.
References (24)
- et al.
A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement
Neuromuscul. Disord.
(2012) - et al.
A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene
Int. J. Cardiol.
(2016) - et al.
A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death
J. Card. Fail.
(2015) - et al.
Expanding the phenotype of sudden cardiac death — an unusual presentation of a family with a Lamin A/C mutation
Int. J. Cardiol.
(2010) - et al.
Congenital fiber type disproportion myopathy caused by LMNA mutations
J. Neurol. Sci.
(2014) - et al.
Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene
Int. J. Cardiol.
(2010) - et al.
A case of lamin A/C mutation cardiomyopathy with overlap features of ARVC: a critical role of genetic testing
Int. J. Cardiol.
(2013) - et al.
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations
Am. J. Cardiol.
(2004) - et al.
Cardioembolic stroke related to limb-girdle muscular dystrophy 1B
BMC Res. Notes
(Jan 29 2013) - et al.
Nuclear envelope-related lipodystrophies
Semin. Cell Dev. Biol.
(2014)
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