Research output

  1. KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers

    Research output: Contribution to journalArticleAcademicpeer-review

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ID: 100033