Long Noncoding RNA Can Be a Probable Mechanism and a Novel Target for Diagnosis and Therapy in Fragile X Syndrome

Fragile X syndrome (FXS) is the most common congenital hereditary disease of low intelligence after Down syndrome. Its main pathogenic gene is fragile X mental retardation 1 (FMR1) gene associated with intellectual disability, autism, and fragile X-related primary ovarian insufficiency (FXPOI) and f...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Ge, Zhu, He, Wu, Shuying, Cui, Manhua, Xu, Tianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541098/
https://www.ncbi.nlm.nih.gov/pubmed/31191598
http://dx.doi.org/10.3389/fgene.2019.00446

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541098/
https://www.ncbi.nlm.nih.gov/pubmed/31191598
http://dx.doi.org/10.3389/fgene.2019.00446

Ejemplares similares