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The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms

Defects in the XPG DNA repair endonuclease gene can result in the cancer-prone disorders xeroderma pigmentosum (XP) or the XP–Cockayne syndrome complex. While the XPG cDNA sequence was known, determination of the genomic sequence was required to understand its different functions. In cells from norm...

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Bibliografiske detaljer
Main Authors: Emmert, Steffen, Schneider, Thomas D., Khan, Sikandar G., Kraemer, Kenneth H.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2001
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC31292/
https://ncbi.nlm.nih.gov/pubmed/11266544
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