Investigating cell-specific effects of FMRP deficiency on spiny projection neurons in a mouse model...
Investigating cell-specific effects of FMRP deficiency on spiny projection neurons in a mouse model of Fragile X syndrome
About this item
Full title
Author / Creator
Publisher
Switzerland: Frontiers
Journal title
Language
English
Formats
Publication information
Publisher
Switzerland: Frontiers
Subjects
More information
Scope and Contents
Contents
Fragile X syndrome (FXS), resulting from a mutation in the
gene, is the most common monogenic cause of autism and inherited intellectual disability.
encodes the Fragile X Messenger Ribonucleoprotein (FMRP), and its absence leads to cognitive, emotional, and social deficits compatible with the nucleus accumbens (NAc) dysfunction. This structur...
Alternative Titles
Full title
Investigating cell-specific effects of FMRP deficiency on spiny projection neurons in a mouse model of Fragile X syndrome
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_023fb8e55c594ba88a765f87d5f20c0f
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_023fb8e55c594ba88a765f87d5f20c0f
Other Identifiers
ISSN
1662-5102
E-ISSN
1662-5102
DOI
10.3389/fncel.2023.1146647
