Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?
SourceSeminars in Immunopathology, 37, 4, (2015), pp. 371-376
Article / Letter to editor
Display more detailsDisplay less details
Seminars in Immunopathology
SubjectRadboudumc 5: Inflammatory diseases RIMLS: Radboud Institute for Molecular Life Sciences
Mevalonate kinase deficiency or hyper-IgD syndrome is a hereditary autoinflammatory syndrome caused by mutations in the mevalonate kinase gene. In this review, we will discuss new findings in this disorder that have been published in the last 2 years. This includes new insights into pathophysiology, treatment, and the clinical phenotype linked to the genetic defect.
Upload full text
Use your RU credentials (u/z-number and password) tolog in with SURFconextto upload a file for processing by the repository team.