No rare deleterious variants from STK32B...

Neurology: Genetics 2017 / 10 Vol. 3; Iss. 5

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, Sylva
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Volume:
3
Language:
english
Journal:
Neurology Genetics
DOI:
10.1212/NXG.0000000000000195
Date:
October, 2017
File:
PDF, 181 KB
english, 2017
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