A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening. (13th March 2019)

Record Type:: Journal Article
Title:: A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening. (13th March 2019)
Main Title:: A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening
Authors:: Mohanty, Purvi
Jadhav, Prajakta
Shanmukhaiah, Chandrakala
Kumar, Selvaa
Vundinti, Babu Rao
Abstract:
Is Part Of:: International journal of dermatology. Volume 58:Number 12(2019)
Journal:: International journal of dermatology
Issue:: Volume 58:Number 12(2019)
Issue Display:: Volume 58, Issue 12 (2019)
Year:: 2019
Volume:: 58
Issue:: 12
Issue Sort Value:: 2019-0058-0012-0000
Page Start:: 1468
Page End:: 1471
Publication Date:: 2019-03-13
Subjects:: Dermatology -- Periodicals
616.5
Journal URLs:: http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=ijd ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ijd.14424 ↗
Languages:: English
ISSNs:: 0011-9059
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4542.185000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 16304.xml