High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung’s disease-Reference-Cited by-同舟云学术

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High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung’s disease

Published:2024-01-22 Issue:1 Volume:40 Page:
ISSN:1437-9813
Container-title:Pediatric Surgery International
language:en
Short-container-title:Pediatr Surg Int

Author:

Ding Hui-yang,Lei Wen,Xiao Shang-jie,Deng Hua,Yuan Li-ke,Xu Lu,Zhou Jia-liang,Huang Rong,Fang Yuan-long,Wang Qing-yuan,Zhang Ying,Zhang Liang,Zhu Xiao-chun

Funder

the Science and Technology Program of Guangzhou

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s00383-023-05620-w.pdf

Reference37 articles.

1. Borrego S, Ruiz-Ferrer M, Fernandez RM et al (2013) Hirschsprung’s disease as a model of complex genetic etiology. Histol Histopathol 28(9):1117–1136. https://doi.org/10.14670/HH-28.1117

2. Karim A, Tang CS, Tam PK (2021) The emerging genetic landscape of hirschsprung disease and its potential clinical applications. Front Pediatr 9:638093. https://doi.org/10.3389/fped.2021.638093

3. Butler TN, Trainor PA (2013) The developmental etiology and pathogenesis of Hirschsprung disease. Transl Res 162(1):1–15. https://doi.org/10.1016/j.trsl.2013.03.001

4. Bodian M, Carter CO, Ward BC (1951) Hirschsprung’s disease. Lancet 1(6650):302–309. https://doi.org/10.1016/s0140-6736(51)92290-8

5. Tilghman JM, Ling AY, Turner TN et al (2019) Molecular genetic anatomy and risk profile of Hirschsprung’s disease. New Engl J Med 380(15):1421–1432. https://doi.org/10.1056/NEJMoa1706594

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