Insight into learning via 'friend of fragile X' gene

(Emory Health Sciences) Fragile X syndrome, caused by a disruption of the gene FMR1, is the most common inherited form of intellectual disability. Emory scientists have revealed new aspects of the function of FMR1 and a 'friend' -- called ZC3H14 in humans/mice and dNab2 in flies.
Source: EurekAlert! - Medicine and Health - Category: International Medicine & Public Health Source Type: news