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ERCC1 is required for FANCD2 focus formation
The rare genetic disorder Fanconi anemia, caused by a deficiency in any of at least thirteen identified genes, is characterized by cellular sensitivity to DNA interstrand crosslinks and genome instability. The excision repair cross complementing protein, ERCC1, first identified as a participant in n...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2575046/ https://ncbi.nlm.nih.gov/pubmed/18672388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2008.06.009 |
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