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Should we perform systematic electrophysiological study in Steinert's disease?
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,...
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| Formato: | Texto |
| Lenguaje: | English |
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BioMed Central
2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576248/ https://www.ncbi.nlm.nih.gov/pubmed/18928563 http://dx.doi.org/10.1186/1749-8090-3-56 |