Article
Physiological regulation and social-emotional processing in female carriers of the FMR1 premutation.
Physiology & behavior - 1 Feb 2020
Winston Molly, Nayar Kritika, Hogan Abigail L, Barstein Jamie, La Valle Chelsea, Sharp Kevin, Berry-Kravis Elizabeth, Losh Molly
Abstract excerpt
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 carriers of the gene in its premutation state. Because the FMR1 premutation is relatively common among women (as high as 1...
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