Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders

Chromosome 15 (C15) imprinting disorders including Prader–Willi (PWS), Angelman (AS) and chromosome 15 duplication (Dup15q) syndromes are severe neurodevelopmental disorders caused by abnormal expression of genes from the 15q11–q13 region, associated with abnormal DNA methylation and/or copy number...

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Detalles Bibliográficos
Autores principales: Baker, Emma K., Butler, Merlin G., Hartin, Samantha N., Ling, Ling, Bui, Minh, Francis, David, Rogers, Carolyn, Field, Michael J., Slee, Jennie, Gamage, Dinusha, Amor, David J., Godler, David E.
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/PMC7595031/
https://www.ncbi.nlm.nih.gov/pubmed/33116122
http://dx.doi.org/10.1038/s41398-020-01034-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595031/
https://www.ncbi.nlm.nih.gov/pubmed/33116122
http://dx.doi.org/10.1038/s41398-020-01034-7

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