Cargando…
Identification of key biomarkers in Angelman syndrome by a multi-cohort analysis
The Angelman Syndrome (AS) is an extreme neurodevelopmental disorder without effective treatments. While most patients with this disease can be diagnosed by genetic testing, there are still a handful of patients have an unrecognized genetic cause for their illness. Thus, novel approaches to clinical...
Autores principales: | Li, Yong, Shu, Junhua, Cheng, Ying, Zhou, Xiaoqing, Huang, Tao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424609/ https://www.ncbi.nlm.nih.gov/pubmed/36052323 http://dx.doi.org/10.3389/fmed.2022.963883 |
Ejemplares similares
-
Genotype–Phenotype Correlations in Angelman Syndrome
por: Yang, Lili, et al.
Publicado: (2021) -
Angelman Syndrome and Angelman-like Syndromes Share the Same Calcium-Related Gene Signatures
por: Panov, Julia, et al.
Publicado: (2021) -
Evaluation of electroencephalography biomarkers for Angelman syndrome during overnight sleep
por: Levin, Yuval, et al.
Publicado: (2022) -
Case Report: A Severe SARS-CoV-2 Infection in a Teenager With Angelman Syndrome
por: Lopes, Alessandra G. D., et al.
Publicado: (2021) -
Epilepsy in patients with Angelman syndrome
por: Fiumara, Agata, et al.
Publicado: (2010)