A case of Schöpf‐Schulz‐Passarge syndrome caused by c.1135C>T WNT10A missense mutation. (15th February 2017)

Record Type:: Journal Article
Title:: A case of Schöpf‐Schulz‐Passarge syndrome caused by c.1135C>T WNT10A missense mutation. (15th February 2017)
Main Title:: A case of Schöpf‐Schulz‐Passarge syndrome caused by c.1135C>T WNT10A missense mutation
Authors:: Painsi, Clemens
Aubell, Kristina
Wolf, Peter
Hügel, Rainer
Lange‐Asschenfeldt, Bernhard
Abstract:
Is Part Of:: Journal der Deutschen Dermatologischen Gesellschaft. Volume 15:Number 4(2017)
Journal:: Journal der Deutschen Dermatologischen Gesellschaft
Issue:: Volume 15:Number 4(2017)
Issue Display:: Volume 15, Issue 4 (2017)
Year:: 2017
Volume:: 15
Issue:: 4
Issue Sort Value:: 2017-0015-0004-0000
Page Start:: 455
Page End:: 457
Publication Date:: 2017-02-15
Subjects:: Skin -- Diseases -- Periodicals
Dermatology -- Periodicals
616.5005
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ddg.13183 ↗
Languages:: English
ISSNs:: 1610-0379
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4663.460655
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 225.xml