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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:PLoS One
Principais autores: Gasca-Salas, Carmen, Masellis, Mario, Khoo, Edwin, Shah, Binit B., Fisman, David, Lang, Anthony E., Kleiner-Fisman, Galit
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4839564/
https://ncbi.nlm.nih.gov/pubmed/27100392
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0153852
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registros relacionados