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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Detalhes bibliográficos
Main Authors: Kaivorinne, Anna-Lotta, Krüger, Johanna, Kuivaniemi, Katja, Tuominen, Hannu, Moilanen, Virpi, Majamaa, Kari, Remes, Anne M
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2008
Assuntos:
Research Article
Acesso em linha: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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