t/gene-cdkl5

CDKL5 gene

Discuss publications and research concerning the CDKL5 gene.

0 members0 posts30 articles

Start the first discussion

Ask a question, share context or link a publication.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details