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COMT Val158Met Polymorphism Modulates Huntington's Disease ProgressionPLoS ONE, 2016, 11 (9), pp.e0161106. ⟨10.1371/journal.pone.0161106⟩
Journal articles
hal-02326563v1
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Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.Archives of Neurology -Chigago-, 2008, 65 (7), pp.958-62. ⟨10.1001/archneur.65.7.958⟩
Journal articles
inserm-00357160v1
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SPG11 spastic paraplegia : A new cause of juvenile parkinsonism.Deutsche Zeitschrift für Nervenheilkunde / Deutsche Zeitschrift f ur Nervenheilkunde, 2009, 256 (1), pp.104-8. ⟨10.1007/s00415-009-0083-3⟩
Journal articles
istex
inserm-00370093v1
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Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H.Neuromuscular Disorders, 2009, 19 (4), pp.255-60. ⟨10.1016/j.nmd.2009.02.003⟩
Journal articles
istex
inserm-00383333v1
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