Nasu-Hakola disease with a splicing mutation of TREM2 in a Japanese family
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2010.03311.x/fullpdf
Reference8 articles.
1. Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy-PLOSL): a dementia associated with bone cystic lesions. From clinical to genetic and molecular aspects;Bianchin;Cell Mol Neurobiol,2004
2. The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2;Klünemann;Neurology,2005
3. Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype;Paloneva;Am J Hum Genet,2002
4. An Italian family with Nasu-Hakola disease;Salmaggi;J Neurol,2003
5. An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the TREM2 gene;Soragna;J Neurol Neurosurg Psychiatry,2003
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