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They also offer a more diverse range of vitamins, minerals and other nutrients than single types
People with polymerase eta pathogenic variants have the same cutaneous and ocular findings as other XP patients but do not have progressive neurologic degeneration.[65] A founder pathogenic variant resulting in a deletion of exon 10 was seen in 16 of 16 individuals from ten Tunisian consanguineous families.[66] Work on genotype-phenotype correlations among the XP complementation groups continues
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