Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease
Authors:
- Pieter C. van Voorst VaderPVPieter C. van Voorst Vader
- Jos W. SnoekJSJos W. Snoek
- Anja RaamsARAnja Raams
- Nicolaas G.J. JaspersNJNicolaas G.J. Jaspers
- Wim J. KleijerWKWim J. Kleijer
- 1 May 1998
- journal article
- case report
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 110 (5) , 832-836
Abstract
No abstract availableKeywords
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