A novel compound heterozygous mutation in DGKE in a Chinese patient causes atypical hemolytic uremic syndrome-Reference-Cited by-同舟云学术

A novel compound heterozygous mutation in DGKE in a Chinese patient causes atypical hemolytic uremic syndrome

Published:2020-01-01 Issue:1 Volume:25 Page:101-107
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Li Jitong¹²,Song Yinsen²,Zhang Yaodong²,Li Hongjiang¹,Tian Ming¹,Li Di¹,Zhang Shufeng¹,Cao Guanghai¹,Liu Cuihua¹

Affiliation:

1. Department of Nephrology and Rheumatology, Affiliated Children’s Hospital of Zhengzhou University, Zhengzhou, People’s Republic of China

2. Henan Provincial Key Laboratory of Children’s Genetics and Metabolic Diseases, Affiliated Children’s Hospital of Zhengzhou University, Zhengzhou, People’s Republic of China

Funder

Science and Technology Department of Henan Province

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/16078454.2020.1731969

Reference30 articles.

1. Atypical hemolytic uremic syndrome

2. Atypical Hemolytic–Uremic Syndrome

3. Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome

4. An international consensus approach to the management of atypical hemolytic uremic syndrome in children

5. Familial haemolytic uraemic syndrome and an MCP mutation

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