Report of a child with sporadic familial progressive hyper‐ and hypopigmentation caused by a novel KITLG mutation. (1st December 2016)

Record Type:: Journal Article
Title:: Report of a child with sporadic familial progressive hyper‐ and hypopigmentation caused by a novel KITLG mutation. (1st December 2016)
Main Title:: Report of a child with sporadic familial progressive hyper‐ and hypopigmentation caused by a novel KITLG mutation
Authors:: Zhang, J.
Cheng, R.
Liang, J.
Ni, C.
Li, M.
Yao, Z.
Abstract:
Is Part Of:: British journal of dermatology. Volume 175:Number 6(2016)
Journal:: British journal of dermatology
Issue:: Volume 175:Number 6(2016)
Issue Display:: Volume 175, Issue 6 (2016)
Year:: 2016
Volume:: 175
Issue:: 6
Issue Sort Value:: 2016-0175-0006-0000
Page Start:: 1369
Page End:: 1371
Publication Date:: 2016-12-01
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.14694 ↗
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:: 24793.xml