Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect.
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| Title: | Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect. |
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| Authors: | Olley G; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK., Pradeepa MM; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK.; Blizard institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK., Grimes GR; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK., Piquet S; Epigenetics and Cell Fate Centre, UMR7216 CNRS, Université de Paris, Paris, France., Polo SE; Epigenetics and Cell Fate Centre, UMR7216 CNRS, Université de Paris, Paris, France., FitzPatrick DR; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK., Bickmore WA; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK. Wendy.Bickmore@igmm.ed.ac.uk., Boumendil C; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Crewe Road, Edinburgh, UK. Charlene.BOUMENDIL@ijm.fr.; Université de Paris, CNRS, Institut Jacques Monod, Paris, France. Charlene.BOUMENDIL@ijm.fr. |
| Source: | Nature communications [Nat Commun] 2021 May 25; Vol. 12 (1), pp. 3127. Date of Electronic Publication: 2021 May 25. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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