Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome. (1st October 2020)

Record Type:: Journal Article
Title:: Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome. (1st October 2020)
Main Title:: Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome
Authors:: Ralser, D.J.
Kumar, S.
Borisov, O.
Sarig, O.
Richard, G.
Wolf, S.
Krawitz, P.M.
Sprecher, E.
Kreiß, M.
Betz, R.C.
Abstract:
Is Part Of:: British journal of dermatology. Volume 183:Number 4(2020)
Journal:: British journal of dermatology
Issue:: Volume 183:Number 4(2020)
Issue Display:: Volume 183, Issue 4 (2020)
Year:: 2020
Volume:: 183
Issue:: 4
Issue Sort Value:: 2020-0183-0004-0000
Page Start:: 756
Page End:: 757
Publication Date:: 2020-10-01
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.19123 ↗
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:: 24799.xml