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Insight into learning via 'friend of fragile X' gene

20:00 EDT 8 Aug 2017 | AAAS

(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.

Original Article: Insight into learning via 'friend of fragile X' gene

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Bioinformatics is the application of computer software and hardware to the management of biological data to create useful information. Computers are used to gather, store, analyze and integrate biological and genetic information which can then be applied...