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You searched for: Author/Creator Houle, Gabrielle

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1. Characterization of the phenotype with cognitive impairment and protein mislocalization in SCA34. (April 2020)

3. Exome-wide rare variant analysis in familial essential tremor. (January 2021)

6. Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor. Issue 7 (6th April 2020)

7. No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremor. (October 2017)

8. SYNE1 mutations cause autosomal‐recessive ataxia with retained reflexes in Brazilian patients. Issue 11 (27th September 2016)

9. Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population. Issue 2 (3rd February 2017)