Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome-Reference-Cited by-同舟云学术

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome

Published:2015-04-08 Issue:6 Volume:10 Page:1011-1019
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Mele Caterina,Lemaire Mathieu,Iatropoulos Paraskevas,Piras Rossella,Bresin Elena,Bettoni Serena,Bick David,Helbling Daniel,Veith Regan,Valoti Elisabetta,Donadelli Roberta,Murer Luisa,Neunhäuserer Maria,Breno Matteo,Frémeaux-Bacchi Véronique,Lifton Richard,Remuzzi Giuseppe,Noris Marina

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Reference30 articles.

1. Atypical Hemolytic–Uremic Syndrome

2. Hemolytic uremic syndrome

3. Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

4. Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults

5. Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

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