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triés par
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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association studyThe Lancet Neurology, 2017, 16 (9), pp.701-711. ⟨10.1016/S1474-4422(17)30161-8⟩
Article dans une revue
hal-04073171v1
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New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-SaguenayAnnals of Neurology, 2015, 78 (6), pp.871-886. ⟨10.1002/ana.24509⟩
Article dans une revue
istex
hal-01955612v1
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Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression.Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.173. ⟨10.1186/1750-1172-8-173⟩
Article dans une revue
inserm-00907850v1
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