Cell migration is impaired in XPA‐deficient cells
Abstract Xeroderma pigmentosum (XP) is a hereditary disorder characterized by photosensitivity, predisposition to skin cancers, and neurological abnormalities including microcephaly and progressive neurodegeneration. A lack of nucleotide excision repair (NER) in patients with XP can cause hypersensi...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2023-02-01
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Series: | FASEB BioAdvances |
Online Access: | https://doi.org/10.1096/fba.2022-00084 |