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Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1
BACKGROUND: Myotonic dystrophy type 1 (DM1) represents a multisystemic disorder in which diffuse brain white and gray matter alterations related to clinical and genetic features have been described. We aimed to evaluate in the brain of adult patients with DM1 (i) white and gray matter differences, i...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4900512/ https://www.ncbi.nlm.nih.gov/pubmed/27330968 http://dx.doi.org/10.1016/j.nicl.2016.04.012 |