rs5848 Polymorphism and Serum Progranulin Level

OBJECTIVE: To assess the influence of rs5848 polymorphism in serum progranulin (PGRN) level in a cohort of subjects with Alzheimer and related dementias from a tertiary referral clinic. BACKGROUND: Mutations in the GRN gene cause autosomal dominant frontotemporal dementia (FTD) with TDP-43 pathology...

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Autors principals: Hsiung, Ging-Yuek R., Fok, Alice, Feldman, Howard H., Rademakers, Rosa, Mackenzie, Ian R.A.
Format: Artigo
Idioma:Inglês
Publicat: 2010
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3085023/
https://ncbi.nlm.nih.gov/pubmed/21047645
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jns.2010.10.009
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