Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.

Xeroderma pigmentosum (XP) and Cockayne syndrome (CS) are two rare inherited disorders with a clinical and cellular hypersensitivity to the UV component of the sunlight spectrum. Although the two traits are generally considered as clinically and genetically distinct entities, on the biochemical leve...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Vermeulen, W, Jaeken, J, Jaspers, N G, Bootsma, D, Hoeijmakers, J H
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1993
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682247/
https://ncbi.nlm.nih.gov/pubmed/8317483
Etiketak: Etiketa erantsi
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