No rare deleterious variants from
<i>STK32B</i>
,
<i>PPARGC1A</i>
, and
<i>CTNNA3</i>
are associated with essential tremor

No rare deleterious variants from STK32B , PPARGC1A , and CTNNA3 are associated with essential tremor

Houle, Gabrielle; Ambalavanan, Amirthagowri; Schmouth, Jean-François; Leblond, Claire S.; Spiegelman, Dan; Laurent, Sandra B.; Bourassa, Cynthia V.; Grayson, Celene; Panisset, Michel; Chouinard, Sylvain; Dupré, Nicolas; Vilariño-Güell, Carles; Rajput, Alex; Girard, Simon L.; Dion, Patrick A.; Rouleau, Guy A.

期刊名称Neurology Genetics
作者Houle, Gabrielle; Ambalavanan, Amirthagowri; Schmouth, Jean-François; Leblond, Claire S.; Spiegelman, Dan; Laurent, Sandra B.; Bourassa, Cynthia V.; Grayson, Celene; Panisset, Michel; Chouinard, Sylvain; Dupré, Nicolas; Vilariño-Güell, Carles; Rajput, Alex; Girard, Simon L.; Dion, Patrick A.; Rouleau, Guy A.
卷第3卷
期第5期
电子ISSN2376-7839
文件大小181.27KB
发表时间2017-10
DOI10.1212/NXG.0000000000000195

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No rare deleterious variants from STK32B , PPARGC1A , and CTNNA3 are associated with essential tremor