Gan Sun

Ministry Of Education Key Laboratory Of Child Development And Disorders, Chongqing Key Laboratory Of Child Infection And Immunity
Chongqing, China

Last Updated: 09/26/2026

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Found 12 publications

X-linked Deficiency in ELF4 in Females with Skewed X Chromosome Inactivation.

X-linked Deficiency in ELF4 in Females with Skewed X Chromosome Inactivation.

Journal: Journal of clinical immunology

Published: September 13, 2024

A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia.

A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia.

Journal: Clinical immunology (Orlando, Fla.)

Published: August 01, 2023

An early-onset SLE patient with a novel paternal inherited BACH2 mutation.

An early-onset SLE patient with a novel paternal inherited BACH2 mutation.

Journal: Journal of clinical immunology

Published: February 26, 2023

Correction to: De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE‑1 Element Insertion Resulting in Chronic Granulomatous Disease.

Correction to: De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE‑1 Element Insertion Resulting in Chronic Granulomatous Disease.

Journal: Journal of clinical immunology

Published: January 20, 2023

A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China.

A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China.

Journal: Journal of clinical immunology

Published: December 30, 2022

Multiple Immune Defects in Two Patients with Novel DOCK2 Mutations Result in Recurrent Multiple Infection Including Live Attenuated Virus Vaccine.

Multiple Immune Defects in Two Patients with Novel DOCK2 Mutations Result in Recurrent Multiple Infection Including Live Attenuated Virus Vaccine.

Journal: Journal of clinical immunology

Published: November 03, 2022

Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes.

Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes.

Journal: Frontiers in immunology

Published: June 19, 2022

De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease.

De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease.

Journal: Journal of clinical immunology

Published: May 27, 2022

Genetic and Functional Identifying of Novel STAT1 Loss-of-Function Mutations in Patients with Diverse Clinical Phenotypes.

Genetic and Functional Identifying of Novel STAT1 Loss-of-Function Mutations in Patients with Diverse Clinical Phenotypes.

Journal: Journal of clinical immunology

Published: February 08, 2022

Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.

Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.

Journal: Journal of clinical immunology

Published: October 30, 2021

Novel mutations of TYK2 leading to divergent clinical phenotypes.

Novel mutations of TYK2 leading to divergent clinical phenotypes.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: May 17, 2021

A Novel Mutation in the NBD Domain of NLRC4 Causes Mild Autoinflammation With Recurrent Urticaria.

A Novel Mutation in the NBD Domain of NLRC4 Causes Mild Autoinflammation With Recurrent Urticaria.

Journal: Frontiers in immunology

Published: March 02, 2021

Showing 1-12 of 12

Last Updated: 09/26/2026