De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies
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DOI: 10.1007/s00439-018-1892-1
Abstract: Intellectual disability (ID) has an estimated prevalence of 1.5–2%. In most affected individuals, its genetic basis remains unclear. Whole exome sequencing (WES) studies have identified a multitude of novel causative gene defects and have shown… read more here.
Keywords: novo fbxo11; behavioural anomalies; intellectual disability; fbxo11 mutations ... See more keywords