Advances in genetic and molecular understanding of Omenn syndrome - implications for the future
Author:
Affiliation:
1. Clinical Resource Building, Floor 4, Block 2, Great North Children’s Hospital, Newcastle Upon Tyne, UK
Funder
National Institute for Health Research Newcastle Biomedical Research Centre
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Link
https://www.tandfonline.com/doi/pdf/10.1080/21678707.2018.1478287
Reference97 articles.
1. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
2. Severe combined immunodeficiencies and related disorders
3. BCG vaccination in patients with severe combined immunodeficiency: Complications, risks, and vaccination policies
4. Newborn Screening for Severe Combined Immunodeficiency in 11 Screening Programs in the United States
5. Successful newborn screening for SCID in the Navajo Nation
Cited by 2 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. Inborn Errors of Immunity With Fetal or Perinatal Clinical Manifestations;Frontiers in Pediatrics;2022-05-06
2. Aproximación diagnóstica ultrasonográfica prenatal al síndrome de Omenn: reporte de caso;Revista Colombiana de Obstetricia y Ginecología;2021-09-30
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