High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia.

Xeroderma pigmentosum (XP) patients in Tunisia who belong to the genetic complementation group A (XPA) have milder skin symptoms than do Japanese XPA patients. Such difference in the clinical features might be caused by the difference in the site of mutation in the XP A-complementing (XPAC) gene. Th...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Nishigori, C, Zghal, M, Yagi, T, Imamura, S, Komoun, M R, Takebe, H
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1993
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682297/
https://ncbi.nlm.nih.gov/pubmed/8105686
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