Associated Papers
Concomitant Ultrarare Mutations in TLR3 and CTPS2 in a Patient with Severe and Recurrent Respiratory Infections in Early Life.
Bougarn S et al.
Journal of Clinical Immunology, 2024
39312089 (PubMed )
Supplement: 10875_2024_1804_MOESM1_ESM.docx
Inborn errors of TLR3- or MDA5-dependent type I IFN immunity in children with enterovirus rhombencephalitis.
Chen J et al.
The Journal of Experimental Medicine, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.
Povysil G et al.
The Journal of Clinical Investigation, 2021
Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.
Povysil G et al.
Medrxiv : the Preprint Server for Health Sciences, 2020
Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis.
Partanen T et al.
Journal of Clinical Immunology, 2020
Recurrent Herpes Zoster Ophthalmicus in a Patient With a Novel Toll-Like Receptor 3 Variant Linked to Compromised Activation Capacity in Fibroblasts.
Liang F et al.
The Journal of Infectious Diseases, 2020
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