New Animal Models for Understanding FMRP Functions and FXS Pathology

Fragile X encompasses a range of genetic conditions, all of which result as a function of changes within the FMR1 gene and abnormal production and/or expression of the FMR1 gene products. Individuals with Fragile X syndrome (FXS), the most common heritable form of intellectual disability, have a ful...

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Detalles Bibliográficos
Autores principales: Curnow, Eliza, Wang, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140010/
https://www.ncbi.nlm.nih.gov/pubmed/35626665
http://dx.doi.org/10.3390/cells11101628

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140010/
https://www.ncbi.nlm.nih.gov/pubmed/35626665
http://dx.doi.org/10.3390/cells11101628

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