Physiological regulation and social-emotional processing in female carriers of the FMR1 premutation

The FMR1 gene is associated with a wide range of clinical and cognitive phenotypes, ranging from intellectual disability and autism symptoms in fragile X syndrome (caused by the FMR1 full mutation), to a more varied, and still poorly understood range of clinical and cognitive phenotypes among carrie...

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Pubblicato in:Physiol Behav
Autori principali: Winston, Molly, Nayar, Kritika, Hogan, Abigail L., Barstein, Jamie, La Valle, Chelsea, Sharp, Kevin, Berry-Kravis, Elizabeth, Losh, Molly
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2019
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6992413/
https://ncbi.nlm.nih.gov/pubmed/31765665
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.physbeh.2019.112746
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