Xeroderma Pigmentosum
Author:
Publisher
Springer Vienna
Link
http://link.springer.com/content/pdf/10.1007/978-3-211-69500-5_51
Reference98 articles.
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4. Arlett CF, Plowman PN, Rogers PB, Parris CN, Abbaszadeh F, Green MH, McMillan TJ, Bush C, Foray N, Lehmann AR (2006) Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum. Br J Radiol 79: 510–517.
5. Bernerd F, Asselineau D, Frechet M, Sarasin A, Magnaldo T (2005) Reconstruction of DNA repair-deficient xeroderma pigmentosum skin in vitro: a model to study hypersensitivity to UV light. Photochem Photobiol 81: 19–24.
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1. Progeroid Cockayne Syndrome;Current Pediatrics;2024-07-10
2. Rare exon 10 deletion in POLH gene in a family with xeroderma pigmentosum variant correlating with protein expression by immunohistochemistry;Giornale Italiano di Dermatologia e Venereologia;2020-07
3. Identification of a novel protein truncating mutation p.Asp98* in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family;Molecular Genetics & Genomic Medicine;2020-01-10
4. Living with xeroderma pigmentosum: comprehensive photoprotection for highly photosensitive patients;Photodermatology, Photoimmunology & Photomedicine;2014-02-19
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