Identification of a novel mutation in CYBB gene in a Chinese neonate with X-linked chronic granulomatous disease-Reference-Cited by-同舟云学术

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Identification of a novel mutation in CYBB gene in a Chinese neonate with X-linked chronic granulomatous disease

Published:2022-03-11 Issue:10 Volume:101 Page:e28875
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Zhang Jie,Fan Meili,Chen Mengmeng,Wang Huihui,Miao Na,Yu Haihua,Zhang Lehai,Deng Qianqian,Yi Changying

Funder

Traditional Chinese Medicine Science and Technology Development Project of Shandong Province

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference16 articles.

1. Chronic granulomatous disease: why an inflammatory disease?;Roxo-Junior;Braz J Med Biol Res,2014

2. Identification of a novel mutation in the CYBB Gene, p.Asp378Gly, in a patient with X-linked chronic granulomatous disease;Song;Allergy Asthma Immunol Res,2014

3. Chronic granulomatous disease: a comprehensive review;Yu;Clin Rev Allergy Immunol,2021

4. Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients;Koker;J Allergy Clin Immunol,2013

5. Clinical and molecular features of 38 children with chronic granulomatous disease in mainland china;Xu;J Clin Immunol,2014

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1. Novel mutations in genes of the IL-12/IFN-γ axis cause susceptibility to tuberculosis;Journal of Infection and Public Health;2023-09

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