Association between polymorphism at codon 469 of the ICAM-1 gene and Henoch-Schönlein purpura in an Iranian cohort-Reference-Cited by-同舟云学术

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Association between polymorphism at codon 469 of the ICAM-1 gene and Henoch-Schönlein purpura in an Iranian cohort

Published:2024-04-27 Issue: Volume: Page:1-8
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Salehi Shima¹,Hozhabrpour Amir²,Takrim Nojehdeh Somayeh³,Mojbafan Marzieh²⁴^ORCID

Affiliation:

1. Department of pediatrics, School of Medicine, Ali-Asghar Children’s Hospital, Iran University of Medical Sciences, Tehran, Iran

2. Department of Medical Genetics, School of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran

3. Dr. Davarnia Genetic Counseling and Diagnosis Center, Imam Reza Hospital, Ardabil, Iran

4. Department of Medical Genetics, School of Medicine, Ali-Asghar Children’s Hospital, Iran University of Medical Sciences, Tehran, Iran

Funder

Iran University of Medical Sciences

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/15257770.2024.2334360

Reference24 articles.

1. Henoch-Schönlein purpura in children and adults: Clinical differences in a defined population

2. New insights in the pathogenesis of immunoglobulin A vasculitis (Henoch-Schönlein purpura)

3. A. Henoch-Schönlein Purpura: A Literature Review;Hetland L. E.;Acta Dermato-Venereologica,2017

4. Genetics of immunoglobulin-A vasculitis (Henoch-Schönlein purpura): An updated review

5. Differential expression of long non‑coding RNA and mRNA in children with Henoch‑Sch�nlein purpura nephritis

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