Group I metabotropic glutamate receptor mediated dynamic immune dysfunction in children with fragile X syndrome

BACKGROUND: Fragile X syndrome (FXS) is the leading cause of inheritable intellectual disability in male children, and is predominantly caused by a single gene mutation resulting in expanded trinucleotide CGG-repeats within the 5’ untranslated region of the fragile X mental retardation (FMR1) gene....

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Detalles Bibliográficos
Autores principales: Careaga, Milo, Noyon, Tamanna, Basuta, Kirin, Van de Water, Judy, Tassone, Flora, Hagerman, Randi J, Ashwood, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107617/
https://www.ncbi.nlm.nih.gov/pubmed/24942544
http://dx.doi.org/10.1186/1742-2094-11-110

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107617/
https://www.ncbi.nlm.nih.gov/pubmed/24942544
http://dx.doi.org/10.1186/1742-2094-11-110

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