Urine microRNA Profiling Displays miR-125a Dysregulation in Children with Fragile X Syndrome

A triplet repeat expansion leading to transcriptional silencing of the FMR1 gene results in fragile X syndrome (FXS), which is a common cause of inherited intellectual disability and autism. Phenotypic variation requires personalized treatment approaches and hampers clinical trials in FXS. We search...

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Detalles Bibliográficos
Autores principales: Putkonen, Noora, Laiho, Asta, Ethell, Doug, Pursiheimo, Juha, Anttonen, Anna-Kaisa, Pitkonen, Juho, Gentile, Adriana M., de Diego-Otero, Yolanda, Castrén, Maija L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072127/
https://www.ncbi.nlm.nih.gov/pubmed/31991700
http://dx.doi.org/10.3390/cells9020289

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072127/
https://www.ncbi.nlm.nih.gov/pubmed/31991700
http://dx.doi.org/10.3390/cells9020289

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