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Editorial | Open Access

A novel structural variant of RET causes familial Hirschsprung’s disease via nonsense-mediated mRNA decay

Qi Wang, Siyu Pu, Bo Xiang( ), Jing Chen( )
Department of Pediatric Surgery and Laboratory of Pediatric Surgery, Rare Diseases Center, Institute of Immunology and Inflammation, Frontiers Science Center for Disease-Related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China

Peer review under responsibility of Chongqing Medical University.

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Genes & Diseases
Volume 11 Issue 1,
January 2024
Pages 7-10
DOI: 10.1016/j.gendis.2023.03.008

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Cite this article:
Wang Q, Pu S, Xiang B, et al. A novel structural variant of RET causes familial Hirschsprung’s disease via nonsense-mediated mRNA decay. Genes & Diseases, 2024, 11(1): 7-10. https://doi.org/10.1016/j.gendis.2023.03.008

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Received: 07 December 2022
Published: 14 April 2023
© 2023 The Authors.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).