Copy number variation analysis using next-generation sequencing identifies the <i>CFHR</i>3/<i>CFHR</i>1 deletion in atypical hemolytic uremic syndrome: a case report-Reference-Cited by-同舟云学术

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Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report

Published:2022-05-26 Issue:1 Volume:27 Page:603-608
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Park Joonhong¹²^ORCID,Yhim Ho-Young³²^ORCID,Kang Kyung Pyo³²^ORCID,Bae Tae Won¹²^ORCID,Cho Yong Gon¹²^ORCID

Affiliation:

1. Department of Laboratory Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, Korea

2. Research Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju, Korea

3. Department of Internal Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, Korea

Funder

National Research Foundation of Korea

Korean government

Publisher

Informa UK Limited

Subject

Hematology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/16078454.2022.2075121

Reference33 articles.

1. Clinico-pathological findings in diarrhoea-negative haemolytic uraemic syndrome

2. Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome

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

4. A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome

5. A radiation hybrid map of complement factor H and factor H-related genes

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