Identification of a Novel Mutation in the CYBB Gene, p.Asp378Gly, in a Patient With X-linked Chronic Granulomatous Disease-Reference-Cited by-同舟云学术

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Identification of a Novel Mutation in the CYBB Gene, p.Asp378Gly, in a Patient With X-linked Chronic Granulomatous Disease

Published:2014 Issue:4 Volume:6 Page:366
ISSN:2092-7355
Container-title:Allergy, Asthma & Immunology Research
language:en
Short-container-title:Allergy Asthma Immunol Res

Author:

Song Sang-Mi¹,Park Mi-Ran¹²,Kim Do-Soo¹²,Kim Jihyun¹²,Kim Yae-Jean¹,Ki Chang-Seok³,Ahn Kangmo¹²

Affiliation:

1. Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

2. Environmental Health Center for Atopic Diseases, Samsung Medical Center, Seoul, Korea.

3. Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Publisher

The Korean Academy of Asthma, Allergy and Clinical Immunology and The Korean Academy of Pediatric Al

Subject

Pulmonary and Respiratory Medicine,Immunology,Immunology and Allergy

Link

https://synapse.koreamed.org/pdf/10.4168/aair.2014.6.4.366

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review;Frontiers in Genetics;2023-01-13

2. Identification of a novel mutation in CYBB gene in a Chinese neonate with X-linked chronic granulomatous disease;Medicine;2022-03-11

3. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update);Blood Cells, Molecules, and Diseases;2021-09

4. Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience;Allergy, Asthma & Immunology Research;2020

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