Associated Papers
CDKL5 Deficiency Disorder (CDD)-Rare Presentation in Male.
Rodak M et al.
Children (basel, Switzerland), 2022
Analysis of X-inactivation status in a Rett syndrome natural history study cohort.
Fang X et al.
Molecular Genetics & Genomic Medicine, 2022
35318820 (PubMed )
Supplement: MGG3-10-e1917-s003.xlsx › Sheet1
Cyclin-Dependent Kinase-Like 5 (CDKL5): Possible Cellular Signalling Targets and Involvement in CDKL5 Deficiency Disorder.
Katayama S et al.
Neural Plasticity, 2020
CDKL5 and ARX mutations in males with early-onset epilepsy.
Mirzaa GM et al.
Pediatric Neurology, 2013
Pathogenic role of the X-linked cyclin-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of life.
Sartori S et al.
Journal of Child Neurology, 2011
MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease.
Kerr M et al.
Molecular Genetics and Metabolism, 0
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