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Preliminary study on the function of the POLD1 (CDC2) EXON2 c.56G>A mutation
BACKGROUND: Fanconi anemia (FA) is a rare recessive disease characterized by DNA damage repair deficiency, and DNA polymerase δ (whose catalytic subunit is encoded by POLD1, also known as CDC2) is closely related to DNA damage repair. Our previous study identified a novel POLD1 missense mutation c.5...
Tallennettuna:
| Julkaisussa: | Mol Genet Genomic Med |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7434749/ https://ncbi.nlm.nih.gov/pubmed/32432416 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1280 |
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