Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia. (1st September 2018)

Record Type:: Journal Article
Title:: Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia. (1st September 2018)
Main Title:: Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia
Authors:: Intarak, N.
Theerapanon, T.
Srijunbarl, A.
Suphapeetiporn, K.
Porntaveetus, T.
Shotelersuk, V.
Abstract:
Is Part Of:: British journal of dermatology. Volume 179:Number 3(2018)
Journal:: British journal of dermatology
Issue:: Volume 179:Number 3(2018)
Issue Display:: Volume 179, Issue 3 (2018)
Year:: 2018
Volume:: 179
Issue:: 3
Issue Sort Value:: 2018-0179-0003-0000
Page Start:: 758
Page End:: 760
Publication Date:: 2018-09-01
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.16541 ↗
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:: 24847.xml