Associated Papers
Blau syndrome NOD2 mutations result in loss of NOD2 cross-regulatory function.
Mao L et al.
Frontiers in Immunology, 2022
Blau syndrome polymorphisms in NOD2 identify nucleotide hydrolysis and helical domain 1 as signalling regulators.
Parkhouse R et al.
Febs Letters, 2014
Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15.
Okada S et al.
Rheumatology (oxford, England), 2009
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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