C.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype. Issue 10 (5th September 2019)
- Record Type:
- Journal Article
- Title:
- C.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype. Issue 10 (5th September 2019)
- Main Title:
- C.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype
- Authors:
- Chen, Shu
Hong, Xiaozhen
Xu, Xianguo
Ma, Kairong
He, Ji
Zhu, Faming - Abstract:
- Is Part Of:
- Transfusion. Volume 59:Issue 10(2019)
- Journal:
- Transfusion
- Issue:
- Volume 59:Issue 10(2019)
- Issue Display:
- Volume 59, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 59
- Issue:
- 10
- Issue Sort Value:
- 2019-0059-0010-0000
- Page Start:
- E4
- Page End:
- E5
- Publication Date:
- 2019-09-05
- Subjects:
- Hematology -- Periodicals
Blood -- Transfusion -- Periodicals
Blood Group Antigens -- Periodicals
Blood Preservation -- Periodicals
Blood Transfusion -- Periodicals
615 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1537-2995 ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=trf ↗
http://www.transfusion.org ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/trf.15496 ↗
- Languages:
- English
- ISSNs:
- 0041-1132
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9020.704000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 17483.xml