LMNA-related dilated cardiomyopathy

A case of idiopathic dilated cardiomyopathy (DCM) that is likely to be associated with LMNA mutation Arg190Pro in a heterozygote is described. The features of DCM in the patient were conduction disorders, cardiac arrhythmias, progressive heart failure and minor musculoskeletal disturbances. We consi...

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Vydáno v:Oxf Med Case Reports
Hlavní autoři: Vaikhanskaya, Tatiyana, Sivitskaya, Larysa, Danilenko, Nina, Davydenko, Oleg, Kurushka, Tatsiyana, Sidorenko, Irina
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2014
Témata:
Case Reports
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4369987/
https://ncbi.nlm.nih.gov/pubmed/25988045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omu040
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