Identification of microRNAs associated with human fragile X syndrome using next-generation sequencing

Fragile X syndrome (FXS) is caused by a mutation in the FMR1 gene which can lead to a loss or shortage of the FMR1 protein. This protein interacts with specific miRNAs and can cause a range of neurological disorders. Therefore, miRNAs could act as a novel class of biomarkers for common CNS diseases....

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Detalles Bibliográficos
Autores principales: Sotoudeh Anvari, Maryam, Vasei, Hamed, Najmabadi, Hossein, Badv, Reza Shervin, Golipour, Akram, Mohammadi-Yeganeh, Samira, Salehi, Saeede, Mohamadi, Mahmood, Goodarzynejad, Hamidreza, Mowla, Seyed Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943156/
https://www.ncbi.nlm.nih.gov/pubmed/35322102
http://dx.doi.org/10.1038/s41598-022-08916-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943156/
https://www.ncbi.nlm.nih.gov/pubmed/35322102
http://dx.doi.org/10.1038/s41598-022-08916-4

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