Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation
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| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2025-01-01
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| Series: | Frontiers in Immunology |
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2024.1544964/full |
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| author | Yu Huang Yu Huang Yu Huang Lu Li Lu Li Ran Chen Ran Chen Lang Yu Lang Yu Shunkai Zhao Yanjun Jia Yanjun Jia Ying Dou Ying Dou Ying Dou Zhiyong Zhang Zhiyong Zhang Yunfei An Yunfei An Xuemei Tang Xuemei Tang Xiaodong Zhao Xiaodong Zhao Lina Zhou |
| author_facet | Yu Huang Yu Huang Yu Huang Lu Li Lu Li Ran Chen Ran Chen Lang Yu Lang Yu Shunkai Zhao Yanjun Jia Yanjun Jia Ying Dou Ying Dou Ying Dou Zhiyong Zhang Zhiyong Zhang Yunfei An Yunfei An Xuemei Tang Xuemei Tang Xiaodong Zhao Xiaodong Zhao Lina Zhou |
| author_sort | Yu Huang |
| collection | DOAJ |
| format | Article |
| id | doaj-art-fc5ca0f511454a53aae326a797ebc629 |
| institution | Kabale University |
| issn | 1664-3224 |
| language | English |
| publishDate | 2025-01-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Immunology |
| spelling | doaj-art-fc5ca0f511454a53aae326a797ebc6292025-01-14T11:55:25ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-01-011510.3389/fimmu.2024.15449641544964Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutationYu Huang0Yu Huang1Yu Huang2Lu Li3Lu Li4Ran Chen5Ran Chen6Lang Yu7Lang Yu8Shunkai Zhao9Yanjun Jia10Yanjun Jia11Ying Dou12Ying Dou13Ying Dou14Zhiyong Zhang15Zhiyong Zhang16Yunfei An17Yunfei An18Xuemei Tang19Xuemei Tang20Xiaodong Zhao21Xiaodong Zhao22Lina Zhou23National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaChongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaDepartment of Hematology Oncology, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaChongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaChongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaChongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaDepartment of Biology, School of Arts and Sciences, Tufts University, Medford, MA, United StatesNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaChongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaChongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaDepartment of Hematology Oncology, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaDepartment of Rheumatism and Immunology, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaDepartment of Rheumatism and Immunology, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaDepartment of Rheumatism and Immunology, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaDepartment of Rheumatism and Immunology, Children’s Hospital of Chongqing Medical University, Chongqing, ChinaNational Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children’s Hospital of Chongqing Medical University, Chongqing, Chinahttps://www.frontiersin.org/articles/10.3389/fimmu.2024.1544964/fullCXCR4 variantgain-of-functioninborn error of immunityWHIM syndromeheterogeneous phenotype |
| spellingShingle | Yu Huang Yu Huang Yu Huang Lu Li Lu Li Ran Chen Ran Chen Lang Yu Lang Yu Shunkai Zhao Yanjun Jia Yanjun Jia Ying Dou Ying Dou Ying Dou Zhiyong Zhang Zhiyong Zhang Yunfei An Yunfei An Xuemei Tang Xuemei Tang Xiaodong Zhao Xiaodong Zhao Lina Zhou Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation Frontiers in Immunology CXCR4 variant gain-of-function inborn error of immunity WHIM syndrome heterogeneous phenotype |
| title | Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation |
| title_full | Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation |
| title_fullStr | Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation |
| title_full_unstemmed | Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation |
| title_short | Corrigendum: Heterogeneous phenotype of a Chinese Familial WHIM syndrome with CXCR4V340fs gain-of-function mutation |
| title_sort | corrigendum heterogeneous phenotype of a chinese familial whim syndrome with cxcr4v340fs gain of function mutation |
| topic | CXCR4 variant gain-of-function inborn error of immunity WHIM syndrome heterogeneous phenotype |
| url | https://www.frontiersin.org/articles/10.3389/fimmu.2024.1544964/full |
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