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

Faber, I; Prota, J R M; Martinez, A R M; Lopes-Cendes, I; França, M C

Faber, I; Prota, J R M; Martinez, A R M; Lopes-Cendes, I; França, M C.

Afiliação

Faber I; Department of Neurology, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.
Prota JR; Department of Medical Genetics, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.
Martinez AR; Department of Neurology, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.
Lopes-Cendes I; Department of Medical Genetics, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.
França MC; Department of Neurology, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, SP, Brazil.

Eur J Neurol ; 24(1): e3-e4, 2017 01.

Article em En | MEDLINE | ID: mdl-28000352

Palavras-chave

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

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Brasil

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