Angelman syndrome genotypes manifest varying degrees of clinical severity and developmental impairment

Angelman Syndrome (AS) is a severe neurodevelopmental disorder due to impaired expression of UBE3A in neurons. There are several genetic mechanisms that impair UBE3A expression, but they differ in how neighboring genes on chromosome 15 at 15q11–q13 are affected. There is evidence that different gene...

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Detalles Bibliográficos
Autores principales: Keute, Marius, Miller, Meghan T., Krishnan, Michelle L., Sadhwani, Anjali, Chamberlain, Stormy, Thibert, Ronald L., Tan, Wen-Hann, Bird, Lynne M., Hipp, Joerg F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505254/
https://www.ncbi.nlm.nih.gov/pubmed/32792659
http://dx.doi.org/10.1038/s41380-020-0858-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505254/
https://www.ncbi.nlm.nih.gov/pubmed/32792659
http://dx.doi.org/10.1038/s41380-020-0858-6

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