2011-02-01
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
Publication
Publication
Nature Genetics , Volume 43 - Issue 2 p. 138- 141
DNA interstrand crosslink repair requires several classes of proteins, including structure-specific endonucleases and Fanconi anemia proteins. SLX4, which coordinates three separate endonucleases, was recently recognized as an important regulator of DNA repair. Here we report the first human individuals found to have biallelic mutations in SLX4. These individuals, who were previously diagnosed as having Fanconi anemia, add SLX4 as an essential component to the FA-BRCA genome maintenance pathway.
Additional Metadata | |
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doi.org/10.1038/ng.751, hdl.handle.net/1765/31609 | |
Nature Genetics | |
Organisation | Erasmus MC: University Medical Center Rotterdam |
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. (2011). SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. Nature Genetics (Vol. 43, pp. 138–141). doi:10.1038/ng.751 |