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
Blau syndrome, clinical and genetic aspects.
Sfriso P et al.
Autoimmunity Reviews, 2012
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