Muscleblind1, but Not Dmpk or Six5, Contributes to a Complex Phenotype of Muscular and Motivational Deficits in Mouse Models of Myotonic Dystrophy

Assessment of molecular defects that underlie cognitive deficits observed in mendelian disorders provides a unique opportunity to identify key regulators of human cognition. Congenital Myotonic Dystrophy 1 (cDM1), a multi-system disorder is characterized by both cognitive deficits and a spectrum of...

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Detalles Bibliográficos
Autores principales: Matynia, Anna, Ng, Carina Hoi, Dansithong, Warunee, Chiang, Andy, Silva, Alcino J., Reddy, Sita
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845609/
https://www.ncbi.nlm.nih.gov/pubmed/20360842
http://dx.doi.org/10.1371/journal.pone.0009857

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845609/
https://www.ncbi.nlm.nih.gov/pubmed/20360842
http://dx.doi.org/10.1371/journal.pone.0009857

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