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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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Functional Analyses of Two Novel LRRK2 Pathogenic Variants in Familial Parkinson's Disease.Movement Disorders, 2022, ⟨10.1002/mds.29124⟩
Article dans une revue
hal-03703786v1
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