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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Detalles Bibliográficos
Autores principales: Guenat, David, Merla, Giuseppe, Deconinck, Eric, Borg, Christophe, Rohrlich, Pierre-Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360356/
https://www.ncbi.nlm.nih.gov/pubmed/28098859
http://dx.doi.org/10.3892/ijmm.2017.2861

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360356/
https://www.ncbi.nlm.nih.gov/pubmed/28098859
http://dx.doi.org/10.3892/ijmm.2017.2861

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