Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis

BACKGROUND: Mutations in granulin (PGRN) and tau (MAPT), and hexanucleotide repeat expansions near the C9orf72 genes are the most prevalent genetic causes of frontotemporal lobar degeneration. Although behavior, language and movement presentations are common, the relationship between genetic subgrou...

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Detalles Bibliográficos
Autores principales: Gasca-Salas, Carmen, Masellis, Mario, Khoo, Edwin, Shah, Binit B., Fisman, David, Lang, Anthony E., Kleiner-Fisman, Galit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839564/
https://www.ncbi.nlm.nih.gov/pubmed/27100392
http://dx.doi.org/10.1371/journal.pone.0153852

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839564/
https://www.ncbi.nlm.nih.gov/pubmed/27100392
http://dx.doi.org/10.1371/journal.pone.0153852

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