Welcome! Click here to login or here to register.
 |
|||||||||||||||||||
|
|||||||||||||||||||
 |
|||||||||||||||||||
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A
|
|
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.
Add your own comment!
There is no comment yet.
|
|
|
|