The TREM2-DAP12 signaling pathway in Nasu–Hakola disease: a molecular genetics perspective

Nasu–Hakola disease or polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL) is a rare recessively inherited disease that is associated with early dementia and bone cysts with fractures. Here, we review the genetic causes of PLOSL with loss-of-function mutations or del...

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Detalles Bibliográficos
Autores principales: Xing, Junjie, Titus, Amanda R, Humphrey, Mary Beth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605443/
https://www.ncbi.nlm.nih.gov/pubmed/26478868
http://dx.doi.org/10.2147/RRBC.S58057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605443/
https://www.ncbi.nlm.nih.gov/pubmed/26478868
http://dx.doi.org/10.2147/RRBC.S58057

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