Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations-Reference-Cited by-同舟云学术

Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations

Published:2012-11-22 Issue:1 Volume:22 Page:24-29
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

Schäfer Annika¹,Hofmann Lars¹,Gratchev Alexei²,Laspe Petra¹,Schubert Steffen¹,Schürer Anke¹,Ohlenbusch Andreas³,Tzvetkov Mladen⁴,Hallermann Christian⁵,Reichrath Jörg⁶,Schön Michael P.¹,Emmert Steffen¹

Affiliation:

1. Department of Dermatology, Venerology and Allergology; University Medical Center Göttingen; Göttingen; Germany

2. Department of Dermatology, Venerology, and Allergology; University Medical Center Mannheim; Mannheim; Germany

3. Department of Pediatrics; University Medical Center Göttingen; Göttingen; Germany

4. Department of Clinical Pharmacology; University Medical Center Göttingen; Göttingen; Germany

5. Department of Dermatology; Fachklinik Hornheide; Münster; Germany

6. Department of Dermatology, Venereology, and Allergology; University Clinic Saarland; Homburg; Germany

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/exd.12052/fullpdf

Reference37 articles.

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

2. Xeroderma Pigmentosum

3. Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

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