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Paper Details

Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome.
Proc Natl Acad Sci U S A
4
2023
FMR1, FMR1 locus, FMR1 mRNA, FMR1 protein, FXTAS, astrocyte, cortical oligodendrocyte lineage, fragile X syndrome, fragile X-associated tremor/ataxia syndrome, glia, glial developmental perturbations, glial populations, human, oligodendrocyte, peripheral blood, premutation, single, trinucleotide
Author NameAffiliation
Biju IssacBoston Children's Hospital
Christopher A WalshManton Center for Orphan Disease Research, Boston Children's Hospital
Christopher A WalshHarvard Medical School
Christopher A WalshBoston Children's Hospital
Christopher A WalshHarvard Medical School
Christopher A WalshManton Center for Orphan Disease Research, Boston Children's Hospital
Christopher A WalshHarvard Medical School
Christopher A WalshBoston Children's Hospital
Christopher A WalshHarvard Medical School
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Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink
Gene OntologyGene Ontology DatabaseLink