Neuropsychiatric feature-based subgrouping reveals neural sensory processing spectrum in female FMR1 premutation carriers: A pilot study

INTRODUCTION: Fragile X Syndrome (FXS) is rare genetic condition characterized by a repeat expansion (CGG) in the Fragile X messenger ribonucleoprotein 1 (FMR1) gene where individuals with greater than 200 repeats are defined as full mutation. FXS clinical presentation often includes intellectual di...

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Detalles Bibliográficos
Autores principales: Norris, Jordan E., Schmitt, Lauren M., De Stefano, Lisa A., Pedapati, Ernest V., Erickson, Craig A., Sweeney, John A., Ethridge, Lauren E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936150/
https://www.ncbi.nlm.nih.gov/pubmed/36816716
http://dx.doi.org/10.3389/fnint.2023.898215

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936150/
https://www.ncbi.nlm.nih.gov/pubmed/36816716
http://dx.doi.org/10.3389/fnint.2023.898215

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