Molecular Biomarkers in Fragile X Syndrome

Fragile X syndrome (FXS) is the most common inherited form of intellectual disability (ID) and a known monogenic cause of autism spectrum disorder (ASD). It is a trinucleotide repeat disorder, in which more than 200 CGG repeats in the 5’ untranslated region (UTR) of the fragile X mental retardation...

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Detalles Bibliográficos
Autores principales: Zafarullah, Marwa, Tassone, Flora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562871/
https://www.ncbi.nlm.nih.gov/pubmed/31035599
http://dx.doi.org/10.3390/brainsci9050096

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562871/
https://www.ncbi.nlm.nih.gov/pubmed/31035599
http://dx.doi.org/10.3390/brainsci9050096

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