Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect

Cornelia de Lange syndrome is a multisystem developmental disorder typically caused by mutations in the gene encoding the cohesin loader NIPBL. The associated phenotype is generally assumed to be the consequence of aberrant transcriptional regulation. Recently, we identified a missense mutation in B...

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Detalles Bibliográficos
Autores principales: Olley, Gabrielle, Pradeepa, Madapura M., Grimes, Graeme R., Piquet, Sandra, Polo, Sophie E., FitzPatrick, David R., Bickmore, Wendy A., Boumendil, Charlene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149872/
https://www.ncbi.nlm.nih.gov/pubmed/34035299
http://dx.doi.org/10.1038/s41467-021-23500-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149872/
https://www.ncbi.nlm.nih.gov/pubmed/34035299
http://dx.doi.org/10.1038/s41467-021-23500-6

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