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COMT Val158Met Polymorphism Modulates Huntington's Disease Progression

Ruth de Diego-Balaguer , Catherine Schramm , Isabelle Rebeix , Emmanuel Dupoux , Alexandra Durr , et al.
PLoS ONE, 2016, 11 (9), pp.e0161106. ⟨10.1371/journal.pone.0161106⟩
Journal articles hal-02326563v1

Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.

Mathieu Anheim , Marie-Celine Fleury , Jerome Franques , Maria-Ceu Moreira , Jean-Pierre Delaunoy , et al.
Archives of Neurology -Chigago-, 2008, 65 (7), pp.958-62. ⟨10.1001/archneur.65.7.958⟩
Journal articles inserm-00357160v1

SPG11 spastic paraplegia : A new cause of juvenile parkinsonism.

Mathieu Anheim , Clotilde Lagier-Tourenne , Giovanni Stevanin , Marie Fleury , Alexandra Durr , et al.
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

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H.

Mireille Cossée , Clotilde Lagier-Tourenne , Claire Seguela , Michel Mohr , France Leturcq , et al.
Neuromuscular Disorders, 2009, 19 (4), pp.255-60. ⟨10.1016/j.nmd.2009.02.003⟩
Journal articles istex inserm-00383333v1