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DNA damage response defect in Williams-Beuren syndrome
Williams-Beuren syndrome (WBS, no. OMIM 194050) is a rare multisystem genetic disorder caused by a microdeletion on chromosome 7q11.23 and characterized by cardiovascular malformations, mental retardation, and a specific facial dysmorphism. Recently, we reported that a series of non-Hodgkin's l...
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| Pubblicato in: | Int J Mol Med |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
D.A. Spandidos
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5360356/ https://ncbi.nlm.nih.gov/pubmed/28098859 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ijmm.2017.2861 |
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