Raising Knowledge and Awareness of Fragile X Syndrome in Serbia, Georgia, and Colombia: A Model for Other Developing Countries?

Fragile X syndrome is the most common monogenetic cause of inherited intellectual disability and syndromic autism spectrum disorder. Fragile X syndrome is caused by an expansion (full mutation ≥200 CGGs repeats, normal 10-45 CGGs) of the fragile X mental retardation 1 (FMR1) gene, epigenetic silenci...

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Detalles Bibliográficos
Autores principales: Protic, Dragana, Salcedo-Arellano, Maria Jimena, Stojkovic, Maja, Saldarriaga, Wilmar, Ávila Vidal, Laura Alejandra, Miller, Robert M., Tabatadze, Nazi, Peric, Marina, Hagerman, Randi, Budimirovic, Dejan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2021
Materias:
Original Contribution
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686783/
https://www.ncbi.nlm.nih.gov/pubmed/34970093

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686783/
https://www.ncbi.nlm.nih.gov/pubmed/34970093

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