Associated Papers
Human early-onset dementia caused by DAP12 deficiency reveals a unique signature of dysregulated microglia.
Zhou Y et al.
Nature Immunology, 2023
Targeted sequencing approach to identify genetic mutations in Nasu-Hakola disease.
Satoh JI et al.
Intractable & Rare Diseases Research, 2016
Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease.
Sasaki A et al.
Neurogenetics, 2015
A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease.
Kuroda R et al.
Journal of the Neurological Sciences, 2007
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