A Causative Relationship between Mutant IFNgR1 Alleles and Impaired Cellular Response to IFNγ in a Compound Heterozygous Child
- 1 March 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (3) , 723-727
- https://doi.org/10.1086/301750
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genomePublished by Elsevier ,2004
- Fatal Disseminated Mycobacterium smegmatis Infection in a Child with Inherited Interferon Receptor DeficiencyClinical Infectious Diseases, 1997
- The gene for the ligand binding chain of the human interferon gamma receptorImmunogenetics, 1997
- Assignment of interferon gamma receptor (IFNGR1) to human chromosome bands 6q24.1→q24.2 by in situ hybridizationCytogenetic and Genome Research, 1997
- Interferon-γ –Receptor Deficiency in an Infant with Fatal Bacille Calmette–Guérin InfectionNew England Journal of Medicine, 1996
- A Mutation in the Interferon-γ –Receptor Gene and Susceptibility to Mycobacterial InfectionNew England Journal of Medicine, 1996
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Two complementation groups account for most cases of inherited MHC class II deficiencyHuman Molecular Genetics, 1994
- Mechanisms of insertional mutagenesis in human genes causing genetic diseaseHuman Genetics, 1991
- Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23–6q24Human Genetics, 1989