Pesquisa da mutação C9ORF72 e de suas características clínicas nos pacientes portadores de esclerose lateral amiotrófica, demência frontotemporal e parkinsonismo atípico

Pesquisa da mutação C9ORF72 e de suas características clínicas nos pacientes portadores de esclerose lateral amiotrófica, demência frontotemporal e parkinsonismo atípico

A descoberta de que a expansão da repetição do hexanucleotídeo GGGGCC no gene C9ORF72 é uma das principais causas da Demência Frontotemporal (DFT) e da Esclerose Lateral Amiotrófica (ELA) foi um importante avanço para o entendimento dessas doenças. Essa mutação é responsável por grande parte dos cas...

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Bibliographic Details
Main Author:	Oliveira, Daniel Sabino de
Other Authors:	Tumas, Vitor
Format:	Others
Language:	pt
Published:	Biblioteca Digitais de Teses e Dissertações da USP 2016
Subjects:	Amyotrophic Lateral Sclerosis Atypical parkinsonism C9ORF72 Demência Frontotemporal Esclerose Lateral Amiotrófica Frontotemporal Dementia Parkinsonismo atípico
Online Access:	http://www.teses.usp.br/teses/disponiveis/17/17161/tde-30032017-135422/

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