Caprin-1
Template:Infobox gene Caprin-1 is a protein that in humans is encoded by the CAPRIN1 gene.[1][2][3][4][5][6] It is suggested that Caprin1 (Template:Aka RNG105) is essential for the formation of long-term memory.[7]
Clinical significance
In 2022, loss-of-function mutations of the CAPRIN1 gene were shown to result in an autosomal-dominant disorder. Patients having the newly-discovered disorder suffer from language impairment, speech delay, intellectual disability, ADHD and autism spectrum disorder.[8] Somatically, they have respiratory problems, limb/skeletal anomalies, developmental delay, feeding difficulties, seizures and ophthalmologic problems.
References
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Further reading
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