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A novel mutation in the XPA gene results in two truncated protein variants and leads to a severe XP/neurological symptoms phenotype

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Bibliographic Details
Main Authors: Lehmann, Janin (Author) , Hänßle, Holger (Author)
Format: Article (Journal)
Language:English
Published: December 2015
In: Journal of the European Academy of Dermatology and Venereology
Year: 2015, Volume: 29, Issue: 12, Pages: 2479-2482
ISSN:1468-3083
DOI:10.1111/jdv.12841
Online Access:Verlag, Volltext: http://dx.doi.org/10.1111/jdv.12841
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Author Notes:J. Lehmann, S. Schubert, A. Schäfer, P. Laspe, H.A. Haenssle, A. Ohlenbusch, A. Gratchev, S. Emmert
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Item Description:Gesehen am 01.07.2016
Physical Description:Online Resource
ISSN:1468-3083
DOI:10.1111/jdv.12841

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