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Rapid Communication | Open Access

The abnormal splicing regulation network caused by synonymous mutations in FBN1 exon 39 leads to Marfan syndrome

Fudan Wua,1, Mingjie Lib,1( ), Xuan Zhoua, Qianyun Wangc, Yan’an Wua( )
Department of Clinical Laboratory, Xiang’an Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian 361102, China
Department of Clinical Laboratory, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, China
Department of Clinical Laboratory, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, Fujian 350000, China

Peer review under the responsibility of the Genes & Diseases Editorial Office, in alliance with the Association of Chinese Americans in Cancer Research (ACACR, Baltimore, MD, USA).

1 These authors contributed equally to this work and were listed as co-first authors.

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Genes & Diseases
Volume 12 Issue 3,
May 2025
Article number: 101371
DOI: 10.1016/j.gendis.2024.101371

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Cite this article:
Wu F, Li M, Zhou X, et al. The abnormal splicing regulation network caused by synonymous mutations in FBN1 exon 39 leads to Marfan syndrome. Genes & Diseases, 2025, 12(3): 101371. https://doi.org/10.1016/j.gendis.2024.101371

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Received: 18 April 2023
Published: 03 July 2024
© 2024 The Authors.

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