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Published in 2019 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms20174075
Abstract: CDKL5 deficiency disorder (CDD) is a severe neurodevelopmental encephalopathy caused by mutations in the X-linked CDKL5 gene that encodes a serine/threonine kinase. CDD is characterised by the early onset of seizures and impaired cognitive and…
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Keywords:
microtubules key;
deficiency disorder;
key understand;
deficiency ... See more keywords