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A new phenotype associated with homozygous GRN mutations: complicated spastic paraplegia
I Faber1, J R M Prota2, A R M Martinez1
1Department of Neurology, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.
European Journal of Neurology
|December 22, 2016
Abstract
No abstract available in PubMed .
Keywords:
GRNataxiaceroid neuronal lipofuscinosisfrontotemporal dementiahereditary spastic paraplegiaprogranulinspastic ataxiaMore Related Videos
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