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  • Title: Should we perform systematic electrophysiological study in Steinert's disease?
    Author: Fayssoil A.
    Journal: J Cardiothorac Surg; 2008 Oct 18; 3():56. PubMed ID: 18928563.
    Abstract:
    Myotonic dystrophy type 1 (Steinert's disease) is a multisystem disorder with autosomal dominant inheritance. This disease is associated with the presence of an abnormal expansion of a cytosine thymine-guanine (CTG) trinucleotide repeat on chromosome 19q13.3. Because of rhythmic complications, the place for systematic electrophysiological study (EPS) has to be discussed.
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