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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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| Publicado no: | Sci Data |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2019
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| Assuntos: | |
| Acesso em linha: | 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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