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...

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Publicat a:Sci Data
Autors principals: De Cegli, Rossella, Iacobacci, Simona, Fedele, Anthony, Ballabio, Andrea, di Bernardo, Diego
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2019
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6834640/
https://ncbi.nlm.nih.gov/pubmed/31695049
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41597-019-0281-5
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