Pathogenesis based Precision Therapy for Inborn Errors of Immunity by SHU Zhou, MAO Huawei

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Research Progress in Diseases Caused by STAT1 Gain-of-Function Mutations by LI Linpeng, MA Jing, GU Hao, SHU Zhou, MAO Huawei

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A Case Report of Aicardi-Goutières Syndrome Type 7 Caused by IFIH1 Gene Mutation and a Literature Review by ZHAO Min, SHU Zhou, HAN Tongxin, FU Yanhua, GAO Tianji, MAO Huawei

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Female CYBB Mutation Mosaicism Leading to Inheritance of X-linked Chronic Granulomatous Disease by ZHANG Yue, SHU Zhou, LI Yan, PIAO Yurong, HAN Tongxin, MAO Huawei

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Successive influenza virus infection and <it>Streptococcus pneumoniae </it>stimulation alter human dendritic cell function by Tu Wenwei, Ho Pak-Leung, Chow Kin-Hung, Ling Man-To, Mao Huawei, Wu Yuet, Lau Yu-Lung

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Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency by Luk, Anderson Dik Wai, Lee, Pamela P., Mao, Huawei, Chan, Koon Wing, Chen, Xiang Yuan, Chen, Tong Xin, He, Jian Xin, Kechout, Nadia, Suri, Deepti, Tao, Yin Bo, Xu, Yong Bin, Jiang, Li Ping, Liew, Woei Kang, Jirapongsananuruk, Orathai, Daengsuwan, Tassalapa, Gupta, Anju, Singh, Surjit, Rawat, Amit, Abdul Latiff, Amir Hamzah, Lee, Anselm Chi Wai, Shek, Lynette P., Nguyen, Thi Van Anh, Chin, Tek Jee, Chien, Yin Hsiu, Latiff, Zarina Abdul, Le, Thi Minh Huong, Le, Nguyen Ngoc Quynh, Lee, Bee Wah, Li, Qiang, Raj, Dinesh, Barbouche, Mohamed-Ridha, Thong, Meow Keong, Ang, Maria Carmen D., Wang, Xiao Chuan, Xu, Chen Guang, Yu, Hai Guo, Yu, Hsin Hui, Lee, Tsz Leung, Yau, Felix Yat Sun, Wong, Wilfred Hing Sang, Tu, Wenwei, Yang, Wangling, Chong, Patrick Chun Yin, Ho, Marco Hok Kung, Lau, Yu Lung