Unusual Disease-Progression in Two Siblings With Xeroderma Pigmentosum Group G

Elena Botta1, Heather Fawcett2, Donata Orioli1

  • 1Institute of Molecular Genetics-CNR, Pavia, Italy.

Clinical Genetics
|January 3, 2026
PubMed
Summary

Protein truncation mutations in the Xeroderma Pigmentosum Group D (XPG) nuclease gene lead to severe disease. However, two siblings with splicing mutations causing in-frame deletions showed a milder clinical phenotype, suggesting a genotype-phenotype correlation.

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