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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Publicado no:Transl Psychiatry
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7595031/
https://ncbi.nlm.nih.gov/pubmed/33116122
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-020-01034-7
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