Combination of Factor H Mutation and Properdin Deficiency Causes Severe C3 Glomerulonephritis-Reference-Cited by-同舟云学术

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Combination of Factor H Mutation and Properdin Deficiency Causes Severe C3 Glomerulonephritis

Published:2012-11-30 Issue:1 Volume:24 Page:53-65
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Lesher Allison M.,Zhou Lin,Kimura Yuko,Sato Sayaka,Gullipalli Damodar,Herbert Andrew P.,Barlow Paul N.,Eberhardt Hannes U.,Skerka Christina,Zipfel Peter F.,Hamano Takayuki,Miwa Takashi,Tung Kenneth S.,Song Wen-Chao

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference50 articles.

1. Complement

2. Complement and its role in innate and adaptive immune responses

3. The spectrum of complement alternative pathway-mediated diseases

4. The Central Role of the Alternative Complement Pathway in Human Disease

5. Membrane complement regulatory proteins

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