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Human USP18 deficiency underlies type 1 interferonopathy ... | ResearchHub
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Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
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Authors
Marije Meuwissen
27 more
Marije Meuwissen
•
Rachel Schot
25 more
•
Grazia Mancini
Published
June 20, 2016
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Journal
The Journal of Experimental Medicine
Topics
Biology
Immunology
Molecular Biology
Inflammation
Genetics
Show all topics
DOI
10.1084/jem.20151529
