A transcriptomic study of Williams-Beuren syndrome associated genes in mouse embryonic stem cells

Williams-Beuren syndrome (WBS) is a relatively rare disease caused by the deletion of 1.5 to 1.8 Mb on chromosome 7 which contains approximately 28 genes. This multisystem disorder is mainly characterized by supravalvular aortic stenosis, mental retardation, and distinctive facial features. We gener...

Descripción completa

Detalles Bibliográficos
Autores principales: De Cegli, Rossella, Iacobacci, Simona, Fedele, Anthony, Ballabio, Andrea, di Bernardo, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Data Descriptor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834640/
https://www.ncbi.nlm.nih.gov/pubmed/31695049
http://dx.doi.org/10.1038/s41597-019-0281-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834640/
https://www.ncbi.nlm.nih.gov/pubmed/31695049
http://dx.doi.org/10.1038/s41597-019-0281-5

Ejemplares similares