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Publications by Agnès Camuzat

A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation

Journal of Alzheimer's Disease
GerontologyClinical PsychologyMental HealthPsychiatryGeriatricsMedicineNeuroscience
2014English

Defining the Spectrum of Frontotemporal Dementias Associated withTARDBPmutations

Neurology: Genetics
NeurologyGenetics
2016English

Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia

Archives of Neurology
2004English

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