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Autor:
B, Bouadjar, F, Aït-Belkacem, L, Daya-Grosjean, A, Sarasin, S L, Larbaoui, R, Ferhat, M C, Cherid, A, Bendissari, A, Chouiter, K, Bouzid, T, Henni, A, Hafiz, A, Allouache, M, Ysmail-Dahlouk
Publikováno v:
Annales de dermatologie et de venereologie. 123(5)
Xeroderma pigmentosum (XP) is a rate autosomal recessive disorder related to DNA repair defects. Recently, modifications of oncogenes and mutations of the p53 suppressor gene have been reported in skin tumors of XP patients. The purpose is to study,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3bffd53bbc1c5088ceea14f620209e4d
https://pubmed.ncbi.nlm.nih.gov/8761081
https://pubmed.ncbi.nlm.nih.gov/8761081
