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XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A
(OMIM ID: #278700 )

Known also as: None


Xeroderma pigmentosum complementation group A (XPA) is caused by mutation in the XPA gene.
Xeroderma pigmentosum is a genetically heterogenous autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Some patients develop neurologic symptoms or a more severe clinical phenotype known as de Sanctis-Cacchione syndrome.


DNA repair proteins related with XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A (#278700 ) disease:
Following keywords are related to XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A:

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

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