Clinical characteristics and epilepsy in genomic imprinting disorders: Angelman syndrome and Prader–Willi syndrome

Angelman syndrome (AS) and Prader–Willi syndrome (PWS) are considered sister imprinting disorders. Although both AS and PWS congenital neurodevelopmental disorders have chromosome 15q11.3-q13 dysfunction, their molecular mechanisms differ owing to genomic imprinting, which results in different paren...

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Detalles Bibliográficos
Autores principales: Wang, Tzong-Shi, Tsai, Wen-Hsin, Tsai, Li-Ping, Wong, Shi-Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137370/
https://www.ncbi.nlm.nih.gov/pubmed/32269945
http://dx.doi.org/10.4103/tcmj.tcmj_103_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137370/
https://www.ncbi.nlm.nih.gov/pubmed/32269945
http://dx.doi.org/10.4103/tcmj.tcmj_103_19

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