Molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uraemic syndrome patients-Reference-Cited by-同舟云学术

Molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uraemic syndrome patients

Published:2019-02-27 Issue:3 Volume:24 Page:357-364
ISSN:1320-5358
Container-title:Nephrology
language:en
Short-container-title:Nephrology

Author:

Jlajla Hend¹²³,Dehman Fatma¹²,Jallouli Manel⁴,Khedher Rania⁵,Ayadi Imen¹²⁶,Zerzeri Yosr¹²,Laadhar Lilia¹²⁶,Sfar Imen⁶⁷,Mahfoudh Abdelmajid⁸,Gorgi Yosr⁶⁷,Cheour Elhem²,Zouaghi Karim⁶⁵,Gargah Tahar⁶⁴,Kallel Sellami Maryam¹²⁶^ORCID

Affiliation:

1. Department of Immunology; La Rabta Hospital; Tunis Tunisia

2. Research Laboratory of Immuno-Rheumatology (LR05 SP01), La Rabta Hospital; Tunis Tunisia

3. Faculty of Sciences; Carthage University; Bizerte Tunisia

4. Department of Paediatrics; Charles Nicolle Hospital; Tunis Tunisia

5. Department of Nephrology; La Rabta Hospital; Tunis Tunisia

6. Faculty of Medicine; El Manar University; Tunis Tunisia

7. Department of Immunology; Charles Nicolle Hospital; Tunis Tunisia

8. Department of Paediatrics; Hedi Chaker Hospital; Sfax Tunisia

Funder

University Tunis El Manar

Publisher