Recurrent deletions of ULK4 in schizophrenia: a gene crucial for neuritogenesis and neuronal motility
Although many pathogenic copy number variations (CNVs) are associated with neuropsychiatric diseases, few of them have been functionally characterised. Here we report multiple schizophrenia cases with CNV abnormalities specific to unc-51-like kinase 4 (ULK4), a serine/threonine kinase gene. Deletion...
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Veröffentlicht in: | Journal of cell science 2014-02, Vol.127 (Pt 3), p.630-640 |
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Sprache: | eng |
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