Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland

BACKGROUND: Frontotemporal lobar degeneration (FTLD) consists of a clinically and neuropathologically heterogeneous group of syndromes affecting the frontal and temporal lobes of the brain. Mutations in microtubule-associated protein tau (MAPT), progranulin (PGRN) and charged multi-vesicular body pr...

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Bibliografische gegevens
Hoofdauteurs: Kaivorinne, Anna-Lotta, Krüger, Johanna, Kuivaniemi, Katja, Tuominen, Hannu, Moilanen, Virpi, Majamaa, Kari, Remes, Anne M
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2008
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2625345/
https://ncbi.nlm.nih.gov/pubmed/19091059
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-8-48
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