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t/gene-cdkl5

CDKL5 gene

Discuss publications and research concerning the CDKL5 gene.

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Related literature

Chromosome X-wide common variant association study in autism spectrum disorder.
CDKL5
CDKL5 deficiency disorder: At the intersection between Rett syndrome and developmental epileptic encephalopathies.
CDKL5
Clinical and functional study of two de novo variations of CDKL5 gene.
CDKL5
Phenotypic characterization of Cdkl5-knockdown neurons establishes elongated cilia as a functional assay for CDKL5 Deficiency Disorder.
CDKL5
Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes.
CDKL5
A novel CDKL5 mutation in a Japanese patient with atypical Rett syndrome.
CDKL5
Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing.
CDKL5
A RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE.
CDKL5
[Early-onset epileptic encephalopathy caused by CDKL5 mutation].
CDKL5
Infantile spasms are associated with abnormal copy number variations.
CDKL5

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