Associated Papers
Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progression.
Garcia-Moreno H et al.
Brain : a Journal of Neurology, 2023
38040034 (PubMed )
Supplement: awad266_supplementary_data.pdf
Brazilian XP-E siblings carrying a novel DDB2 variant developed early-onset melanoma: a case report.
de Souza Timoteo AR et al.
Bmc Medical Genomics, 2023
Expanding molecular roles of UV-DDB: Shining light on genome stability and cancer.
Beecher M et al.
Dna Repair, 2020
Novel mutation identified in the DDB2 gene in patients with xeroderma pigmentosum group-E.
Karagün E et al.
International Journal of Dermatology, 2020
Identification of a novel DDB2 mutation in a Chinese Han family with Xeroderma pigmentosum group E:a case report and literature review.
Yang R et al.
Bmc Medical Genetics, 2020
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