Associated Papers
Clinical Overlapping in Autoinflammatory Diseases: The Role of Gene Duplication.
Galozzi P et al.
Frontiers in Immunology, 2017
Blau syndrome polymorphisms in NOD2 identify nucleotide hydrolysis and helical domain 1 as signalling regulators.
Parkhouse R et al.
Febs Letters, 2014
Blau syndrome, clinical and genetic aspects.
Sfriso P et al.
Autoimmunity Reviews, 2012
A novel mutation in the NOD2 gene associated with Blau syndrome: a Norwegian family with four affected members.
Milman N et al.
Scandinavian Journal of Rheumatology, 0
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