A new phenotype associated with homozygous GRN mutations: complicated spastic paraplegia

Eur J Neurol. 2017 Jan;24(1):e3-e4. doi: 10.1111/ene.13194.

Authors

I Faber¹, J R M Prota², A R M Martinez¹, I Lopes-Cendes², M C França Júnior¹

Affiliations

¹ Department of Neurology, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.
² Department of Medical Genetics, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.

PMID: 28000352
DOI: 10.1111/ene.13194

No abstract available

Keywords: GRN; ataxia; ceroid neuronal lipofuscinosis; frontotemporal dementia; hereditary spastic paraplegia; progranulin; spastic ataxia.

Publication types

Letter