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

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...

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Bibliographic Details
Main Authors: Ge Huang, He Zhu, Shuying Wu, Manhua Cui, Tianmin Xu
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-05-01
Series:Frontiers in Genetics
Subjects:
long noncoding RNA
fragile X syndrome
fragile X-related primary ovarian insufficiency
fragile X-associated tremor/ataxia syndrome
FMR4
FMR6
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2019.00446/full

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https://www.frontiersin.org/article/10.3389/fgene.2019.00446/full

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