Association of Neuregulin 1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C Polymorphisms with Susceptibility to Non-Syndromic Hirschsprung’s Disease-Reference-Cited by-同舟云学术

Association of Neuregulin 1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C Polymorphisms with Susceptibility to Non-Syndromic Hirschsprung’s Disease

Published:2019-11-18 Issue:3 Volume:40 Page:198-205
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Hosseini-Jangjou Seyed Hamed¹,Dastgheib Seyed Alireza²,Aflatoonian Majid³,Amooee Abdolhamid⁴,Bahrami Reza⁵,Salehi Elham⁶,Sadeghizadeh-Yazdi Jalal⁷,Neamatzadeh Hossein⁸⁹

Affiliation:

1. Department of Pediatrics, Shahid Beheshti University of Medical Sciences, Tehran, Iran

2. Department of Medical Genetics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

3. Department of Pediatrics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

4. Department of Surgery, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

5. Neonatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

6. Department of Basic Science, Faculty of Veterinary Medicine, Ardakan University, Ardakan, Iran

7. Department of Food Sciences and Technology, School of Public Health, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

8. Department of Medical Genetics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.;

9. Mother and Newborn Health Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2019.1692113

Reference27 articles.

1. RET and PHOX2B Genetic Polymorphisms and Hirschsprung's Disease Susceptibility: A Meta-Analysis

2. Association of REarranged during Transfection (RET) c.73 + 9277T > C and c.135G > a Polymorphisms with Susceptibility to Hirschsprung Disease: A Systematic Review and Meta-Analysis

3. Hirschsprung disease, associated syndromes and genetics: a review

4. Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease

5. Hirschsprung’s Disease in Newborns

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1. The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung’s disease;Frontiers in Cell and Developmental Biology;2023-07-07

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