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Rapid Communication | Open Access

A novel mutation in the KLHL17 gene is associated with neurodevelopmental disorders

Meng Aoa,1, Shunxiang Zhanga,1, Yun Ouyanga,1, Shucong Lia, Heqian Maa, Meizhen Guoa, Xuelin Daia, Qianhui Xiaa, Xiaoying Zhanga,b,c( )
The School of Public Health, Guilin Medical University, Guilin, Guangxi 541100, China
The Guangxi Key Laboratory of Environmental Exposomics and Entire Lifecycle Heath, Guilin, Guangxi 541199, China
Guangxi Health Commission Key Laboratory of Entire Lifecycle Health and Care, Guilin, Guangxi 541199, China

1 These authors contributed equally to this work.

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).

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Genes & Diseases
Volume 12 Issue 5,
September 2025
Article number: 101528
DOI: 10.1016/j.gendis.2025.101528

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Cite this article:
Ao M, Zhang S, Ouyang Y, et al. A novel mutation in the KLHL17 gene is associated with neurodevelopmental disorders. Genes & Diseases, 2025, 12(5): 101528. https://doi.org/10.1016/j.gendis.2025.101528

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Received: 19 August 2024
Published: 10 January 2025
© 2025 The Authors.

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