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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Detalles Bibliográficos
Autor principal: Fayssoil, Abdallah
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Letters to the Editor
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

Internet

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

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