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[Because several atypical xeroderma pigmentosum (XP) phenotype-causing XPF missense mutations are located in the SLX4-interacting region, we suspected the disruption of the interaction with SLX4 in these XPF mutants, thereby causing severer phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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