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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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Careaga, Milo, Noyon, Tamanna, Basuta, Kirin, Van de Water, Judy, Tassone, Flora, Hagerman, Randi J, Ashwood, Paul
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2014
Sujets:
Research
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4107617/
https://ncbi.nlm.nih.gov/pubmed/24942544
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1742-2094-11-110
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