Repeat-mediated epigenetic dysregulation of the FMR1 gene in the fragile X-related disorders

The fragile X-related disorders are members of the Repeat Expansion Diseases, a group of genetic conditions resulting from an expansion in the size of a tandem repeat tract at a specific genetic locus. The repeat responsible for disease pathology in the fragile X-related disorders is CGG/CCG and the...

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Detalles Bibliográficos
Autores principales: Usdin, Karen, Kumari, Daman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452891/
https://www.ncbi.nlm.nih.gov/pubmed/26089834
http://dx.doi.org/10.3389/fgene.2015.00192

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452891/
https://www.ncbi.nlm.nih.gov/pubmed/26089834
http://dx.doi.org/10.3389/fgene.2015.00192

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