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• W2051981413 abstract "Xeroderma pigmentosum is an extremely rare, autosomal recessive disease characterized by a more than 1000-fold increase in nonmelanoma skin cancer. Individuals with this disease can be divided into eight complementation groups: A-G and V for variant. Each one represents a different genetic defect in DNA repair.To review the molecular basis of xeroderma pigmentosum.Deficiencies in various gene products in the nucleotide excision repair pathway cause xeroderma pigmentosum in complementation groups A-G. The molecular basis of the variant group remains to be elucidated.Research into the genetic defects underlying xeroderma pigmentosum have led to an increased understanding of nucleotide excision repair." @default.
• W2051981413 created "2016-06-24" @default.
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• W2051981413 creator A5039778836 @default.
• W2051981413 creator A5088685303 @default.
• W2051981413 date "1997-06-01" @default.
• W2051981413 modified "2023-10-15" @default.
• W2051981413 title "The Molecular Basis of Xeroderma Pigmentosum" @default.
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• W2051981413 doi "https://doi.org/10.1111/j.1524-4725.1997.tb00084.x" @default.
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