Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype. (September 2017)
- Record Type:
- Journal Article
- Title:
- Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype. (September 2017)
- Main Title:
- Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype
- Authors:
- Leonhardt, Alexandria
Hauer, Jill
Ghiringhelli, Nicolo
Zhang, Yuzhou
Meyer, Nicole
Goodfellow, Renee X.
Martin, Bertha
Nester, Carla
Smith, Richard - Abstract:
- Is Part Of:
- Molecular immunology. Volume 89(2017:Sep.)
- Journal:
- Molecular immunology
- Issue:
- Volume 89(2017:Sep.)
- Issue Display:
- Volume 89 (2017)
- Year:
- 2017
- Volume:
- 89
- Issue Sort Value:
- 2017-0089-0000-0000
- Page Start:
- 175
- Page End:
- 176
- Publication Date:
- 2017-09
- Subjects:
- Immunochemistry -- Periodicals
Molecular biology -- Periodicals
Immunochemistry -- Periodicals
Allergy and Immunology -- Periodicals
Molecular Biology -- Periodicals
Immunochimie -- Périodiques
Biologie moléculaire -- Périodiques
Immunochemistry
Molecular biology
Periodicals
Electronic journals
571.96 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01615890 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.molimm.2017.06.158 ↗
- Languages:
- English
- ISSNs:
- 0161-5890
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817700
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4650.xml