De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures

BACKGROUND: De novo variants in the voltage-gated calcium channel subunit α1 E gene (CACNA1E) have been described as causative of epileptic encephalopathy with contractures, macrocephaly and dyskinesias. METHODS: Following the observation of an index patient with developmental delay and autism spect...

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Detalles Bibliográficos
Autores principales: Royer-Bertrand, Beryl, Jequier Gygax, Marine, Cisarova, Katarina, Rosenfeld, Jill A., Bassetti, Jennifer A., Moldovan, Oana, O’Heir, Emily, Burrage, Lindsay C., Allen, Jake, Emrick, Lisa T., Eastman, Emma, Kumps, Camille, Abbas, Safdar, Van Winckel, Geraldine, Chabane, Nadia, Zackai, Elaine H., Lebon, Sebastien, Keena, Beth, Bhoj, Elizabeth J., Umair, Muhammad, Li, Dong, Donald, Kirsten A., Superti-Furga, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547031/
https://www.ncbi.nlm.nih.gov/pubmed/34702355
http://dx.doi.org/10.1186/s13229-021-00473-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547031/
https://www.ncbi.nlm.nih.gov/pubmed/34702355
http://dx.doi.org/10.1186/s13229-021-00473-3

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