Dystrophia myotonica type 1 presenting with dysarthria: A case report and literature review

Dystrophia myotonica (DM) type 1 is an autosomal dominant disorder, caused by a trinucleotide CTG repeat expansion in the 3′ untranslated region of the dystrophia myotonica protein kinase (DMPK) gene (chromosome 19q13.3). The disorder affects different organ systems, including the skeletal muscles,...

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Detalles Bibliográficos
Autores principales: Li, Chunrong, Zhang, Xiaoling, Zhou, Chunkui, Zhu, Lijun, Liu, Kangding, Fang, Shaokuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5525585/
https://www.ncbi.nlm.nih.gov/pubmed/28810563
http://dx.doi.org/10.3892/etm.2017.4579

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5525585/
https://www.ncbi.nlm.nih.gov/pubmed/28810563
http://dx.doi.org/10.3892/etm.2017.4579

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