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Increased risk of skin cancer in Japanese heterozygotes of xeroderma pigmentosum group A

Journal Article · · Journal of Human Genetics

Not provided.

Research Organization:
National Academy of Sciences, Washington, DC (United States)
Sponsoring Organization:
USDOE Office of Environment, Health, Safety and Security (AU)
DOE Contract Number:
HS0000031
OSTI ID:
1613764
Journal Information:
Journal of Human Genetics, Vol. 63, Issue 11; ISSN 1434-5161
Publisher:
Springer Nature
Country of Publication:
United States
Language:
English

References (7)

Xeroderma pigmentosum - bridging a gap between clinic and laboratory: Xeroderma pigmentosum April 2001
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair November 2010
Characterization of a splicing mutation in group A xeroderma pigmentosum. December 1990
Histologic characteristics of skin cancer in Hiroshima and Nagasaki: Background incidence and radiation effects January 2005
Shining a Light on Xeroderma Pigmentosum March 2012
Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome December 1992
Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population October 2006