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Published in 2018 at "PLoS ONE"
DOI: 10.1371/journal.pone.0196587
Abstract: Mutations in the Cyclin-dependent kinase-like 5 (CDKL5) gene cause severe neurodevelopmental disorders. Recently we have generated Cdkl5 KO mice by targeting exon 2 on the C57BL/6N background, and demonstrated postsynaptic overaccumulation of GluN2B-containing N-methyl-D-aspartate (NMDA)…
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Keywords:
long term;
mice;
cdkl5 mice;
memory ... See more keywords
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Published in 2021 at "Aging and Disease"
DOI: 10.14336/ad.2020.0827
Abstract: CDKL5 deficiency disorder (CDD) is a severe neurodevelopmental disease caused by mutations in the X-linked CDKL5 gene. Children affected by CDD display a clinical phenotype characterized by early-onset epilepsy, intellectual disability, motor impairment, and autistic-like…
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Keywords:
cdkl5 mice;
cdkl5;
decline;
motor ... See more keywords