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Rapid Communication | Open Access

Identification of a splice site mutation in IL2RG in a Chinese boy with X-linked severe combined immunodeficiency

Feng Dinga, He Zhanga, Xiangxiang Liua, Lin Leib, Hongyi Zhangb, Zhichao Liub, Mutong Fangb( ), Shuihua Lua,b( )
National Clinical Research Center for Infectious Diseases, Shenzhen Third People’s Hospital, Shenzhen, Guangdong 518112, China
Shenzhen Third People’s Hospital, The Second Affiliated Hospital, Southern University of Science and Technology, Shenzhen, Guangdong 518112, 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).

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Genes & Diseases
Volume 12 Issue 5,
September 2025
Article number: 101515
DOI: 10.1016/j.gendis.2025.101515

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Cite this article:
Ding F, Zhang H, Liu X, et al. Identification of a splice site mutation in IL2RG in a Chinese boy with X-linked severe combined immunodeficiency. Genes & Diseases, 2025, 12(5): 101515. https://doi.org/10.1016/j.gendis.2025.101515

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Received: 06 May 2024
Published: 04 January 2025
© 2025 The Authors.

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