Fragile X Premutation

Whereas full mutation CGG-repeat expansions (>200 repeats) of the fragile X gene (FMR1) give rise to the neurodevelopmental disorder, fragile X syndrome (FXS); smaller, ‘premutation’ expansions (55 to 200 repeats) are now gaining increasing recognition as the basis for a spectrum of clinical invo...

Descripción completa

Detalles Bibliográficos
Autores principales: Tassone, Flora, Hagerman, Paul J, Hagerman, Randi J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Editorial
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147873/
https://www.ncbi.nlm.nih.gov/pubmed/25170346
http://dx.doi.org/10.1186/1866-1955-6-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147873/
https://www.ncbi.nlm.nih.gov/pubmed/25170346
http://dx.doi.org/10.1186/1866-1955-6-22

Ejemplares similares