LE WE PMID CA
Xeroderma pigmentosum4435Xeroderma pigmentosum

Ataxia teleangiectasia

Bloom s syndrome

Cockayne s syndrome

DNA (Repair and Toxicology)

Hutchinson Gilford syndrome

Progeria

Rothmund Thomson s syndrome

TFIIH

Trichothiodystrophy

Werner s syndrome

Xeroderma pigmentosum

XPG

2003  
1
1994  
2
Oculocutaneous manifestations in xeroderma pigmentosa.
[8199117] Br J Ophthalmol 78(4): 295-7 (1994)
2008  
3
XPG: its products and biological roles.
[19181113] Adv Exp Med Biol 637(-): 83-92 (2008)
2008  
4
2008  
5
Hot topics in DNA repair: the molecular basis for different disease states caused by mutations in TFIIH and XPG.
[18077223] DNA Repair (Amst) 7(2): 339-44 (2008)
2009  
6
From the rarest to the most common: insights from progeroid syndromes into skin cancer and aging.
[19387478] J Invest Dermatol 129(10): 2340-50 (2009)
2007  
7
The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum.
[17184928] Neuroscience 145(4): 1407-17 (2007)
2007  
8
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship.
[17276014] Neuroscience 145(4): 1388-96 (2007)

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