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XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G
(OMIM ID: #278780 )

Known also as: None


Xeroderma pigmentosum complementation group G (XPG) and XPG/Cockayne syndrome are caused by mutation in the ERCC5 gene. For a general description of xeroderma pigmentosum, see XPA, and of Cockayne syndrome. Complementation group G has one of the smallest series of cases.


DNA repair proteins related with XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G (#278780 ) disease:
Following keywords are related to XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G:

Last modification of this entry: Oct. 19, 2010.

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