An unusual mutation in the XPG gene leads to an internal in‐frame deletion and a XP/CS complex phenotype. (26th July 2014)

Record Type:: Journal Article
Title:: An unusual mutation in the XPG gene leads to an internal in‐frame deletion and a XP/CS complex phenotype. (26th July 2014)
Main Title:: An unusual mutation in the XPG gene leads to an internal in‐frame deletion and a XP/CS complex phenotype
Authors:: Lehmann, J.
Schubert, S.
Schäfer, A.
Apel, A.
Laspe, P.
Schiller, S.
Ohlenbusch, A.
Gratchev, A.
Emmert, S.
Abstract:
Is Part Of:: British journal of dermatology. Volume 171:Number 4(2014:Oct.)
Journal:: British journal of dermatology
Issue:: Volume 171:Number 4(2014:Oct.)
Issue Display:: Volume 171, Issue 4 (2014)
Year:: 2014
Volume:: 171
Issue:: 4
Issue Sort Value:: 2014-0171-0004-0000
Page Start:: 903
Page End:: 905
Publication Date:: 2014-07-26
Subjects:: Dermatology -- Periodicals
Skin -- Diseases -- Periodicals
616.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2133 ↗
https://academic.oup.com/bjd ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/bjd.13035 ↗
Languages:: English
ISSNs:: 0007-0963
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 2307.400000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 3788.xml