Xeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities-Reference-Cited by-同舟云学术

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Xeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities

Published:2012-03-15 Issue:4 Volume:21 Page:304-307
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:

Author:

Moriwaki Shinichi,Takigawa Masahiro,Igarashi Naoya,Nagai Yayoi,Amano Hiroo,Ishikawa Osamu,Khan Sikandar G.,Kraemer Kenneth H.

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0625.2012.01446.x/fullpdf

Reference23 articles.

1. Xeroderma Pigmentosum

2. Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair

3. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: A complex genotype–phenotype relationship

4. Xeroderma pigmentosum - bridging a gap between clinic and laboratory

5. Common pathways for ultraviolet skin carcinogenesis in the repair and replication defective groups of xeroderma pigmentosum

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