Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease-Reference-Cited by-同舟云学术

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Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease

Published:1998-05 Issue:5 Volume:110 Page:832-836
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Sijbers Anneke M.,van Voorst Vader Pieter C.,Snoek Jos W.,Raams Anja,Jaspers Nicolaas G.J.,Kleijer Wim J.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference34 articles.

1. Mammalian DNA nucleotide excision repair reconstituted with purified components;Aboussekhra;Cell,1995

2. Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation;Andrews;Proc Natl Acad Sci USA,1978

3. A sixth complementation group in xeroderma pigmentosum;Arase;Mutat Res,1979

4. Liquid-holding recovery of sister chromatid exchanges in UV-irradiated normal and xeroderma pigmentosum complementation groups A and F fibroblasts;Arase;Arch Dermatol Res,1990

5. A case of xeroderma pigmentosum complementation group F;Arase;Hifubyoh-Shinryoh,1988

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