Increased risk of internal tumors in DNA repair-deficient xeroderma pigmentosum patients: analysis of four international cohorts

BACKGROUND: Xeroderma pigmentosum (XP) is a rare, autosomal, recessive DNA repair-deficiency disorder with a frequency of 1–3 per million livebirths in Europe and USA but with higher frequencies in isolated islands or in countries with a high level of consanguinity. XP is characterized by high incid...

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Detalles Bibliográficos
Autores principales: Nikolaev, Sergey, Yurchenko, Andrey A., Sarasin, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896305/
https://www.ncbi.nlm.nih.gov/pubmed/35246173
http://dx.doi.org/10.1186/s13023-022-02203-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896305/
https://www.ncbi.nlm.nih.gov/pubmed/35246173
http://dx.doi.org/10.1186/s13023-022-02203-1

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