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首页|期刊导航|Genes & Diseases|Novel PIK3CG compound heterozygous variants cause inactivated PI3Kγsyndrome presenting as necrotizing enterocolitis in a preterm infant

Novel PIK3CG compound heterozygous variants cause inactivated PI3Kγsyndrome presenting as necrotizing enterocolitis in a preterm infant

Wenting Zhang Xiaoying Zhou Bixia Zheng Xinyi Yang Yongcheng Ni Dong Zhou Chunli Wang

Genes & Diseases2026,Vol.13Issue(2):P.46-49,4.
Genes & Diseases2026,Vol.13Issue(2):P.46-49,4.DOI:10.1016/j.gendis.2025.101618

Novel PIK3CG compound heterozygous variants cause inactivated PI3Kγsyndrome presenting as necrotizing enterocolitis in a preterm infant

Wenting Zhang 1Xiaoying Zhou 2Bixia Zheng 3Xinyi Yang 4Yongcheng Ni 5Dong Zhou 4Chunli Wang3

作者信息

  • 1. Central Laboratory of Pediatrics,Affiliated Changzhou Children''s Hospital of Nantong University,Changzhou,Jiangsu 213003,China Pharmaceutical Laboratory,Asthma and Bronchitis Research Center of Changzhou,Changzhou,Jiangsu 213003,China
  • 2. Central Laboratory of Pediatrics,Affiliated Changzhou Children''s Hospital of Nantong University,Changzhou,Jiangsu 213003,China Department of Neonatology,Affiliated Changzhou Children''s Hospital of Nantong University,Changzhou,Jiangsu 213003,China
  • 3. Nanjing Key Laboratory of Pediatrics,Children''s Hospital of Nanjing Medical University,Nanjing,Jiangsu 210008,China
  • 4. Central Laboratory of Pediatrics,Affiliated Changzhou Children''s Hospital of Nantong University,Changzhou,Jiangsu 213003,China
  • 5. Department of Pediatric Intensive Care,Affiliated Changzhou Children''s Hospital of Nantong University,Changzhou,Jiangsu 213003,China
  • 折叠

摘要

关键词

Necrotizing enterocolitis/Inactivated PI K syndrome/Preterm infant/IPGS/Pik cg/Biallelic loss function variants/Phosphoinositide kinase gamma/Compound heterozygous variants

分类

医药卫生

引用本文复制引用

Wenting Zhang,Xiaoying Zhou,Bixia Zheng,Xinyi Yang,Yongcheng Ni,Dong Zhou,Chunli Wang..Novel PIK3CG compound heterozygous variants cause inactivated PI3Kγsyndrome presenting as necrotizing enterocolitis in a preterm infant[J].Genes & Diseases,2026,13(2):P.46-49,4.

基金项目

supported by the China Postdoctoral Science Foundation(No.2021M700546) (No.2021M700546)

Changzhou Sci&Tech Program(China)(No.CE20235066,CE20225052) (China)

Key project of Changzhou Medical Center Affiliated to Nanjing Medical University(China)(No.CMCM202314) (China)

Clinical Research Project of Nantong University(China)(No.2019LY029). (China)

Genes & Diseases

2352-4820

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