Identification of one Novel complex delins mutation and one recurrent mutation of ERCC8 gene in a Chinese family with Cockayne Syndrome A. (5th April 2017)
- Record Type:
- Journal Article
- Title:
- Identification of one Novel complex delins mutation and one recurrent mutation of ERCC8 gene in a Chinese family with Cockayne Syndrome A. (5th April 2017)
- Main Title:
- Identification of one Novel complex delins mutation and one recurrent mutation of ERCC8 gene in a Chinese family with Cockayne Syndrome A
- Authors:
- Gu, Y.
Bhatta, A.K.
Du, X.
Shao, M.
Keyal, U.
Zhang, G.
Hua, Y. - Abstract:
- Is Part Of:
- Journal of the European Academy of Dermatology and Venereology. Volume 31:Number 9(2017)
- Journal:
- Journal of the European Academy of Dermatology and Venereology
- Issue:
- Volume 31:Number 9(2017)
- Issue Display:
- Volume 31, Issue 9 (2017)
- Year:
- 2017
- Volume:
- 31
- Issue:
- 9
- Issue Sort Value:
- 2017-0031-0009-0000
- Page Start:
- e394
- Page End:
- e395
- Publication Date:
- 2017-04-05
- Subjects:
- Dermatology -- Periodicals
Sexually transmitted diseases -- Periodicals
616.5 - Journal URLs:
- https://onlinelibrary.wiley.com/journal/14683083 ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=jdv ↗
http://www.sciencedirect.com/science/journal/09269959 ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0926-9959;screen=info;ECOIP ↗
http://www.blackwell-synergy.com/loi/jdv ↗ - DOI:
- 10.1111/jdv.14201 ↗
- Languages:
- English
- ISSNs:
- 0926-9959
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4741.624000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4607.xml