Background: Haploinsufficiency A20 (HA20) is a newly described monogenic disease characterized by a wide spectrum of manifestations and caused by heterozygous mutations in TNFAIP3 which encodes A20 pr
Data are mean ± SD or n (%) values. CADASIL cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy nWMHs normalized White Matter Hyperintensities. Demographic and c
