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Comment
. 2015 May 5;112(18):E2269.
doi: 10.1073/pnas.1503756112. Epub 2015 Mar 30.

Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor

Affiliations
Comment

Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor

Hilal Unal Gulsuner et al. Proc Natl Acad Sci U S A. .
No abstract available

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Conflict of interest statement

The authors declare no conflict of interest.

Comment on

References

    1. Unal Gulsuner H, et al. Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. Proc Natl Acad Sci USA. 2014;111(51):18285–18290. - PMC - PubMed
    1. Tzoulis C, et al. HTRA2 p.G399S in Parkinson disease, essential tremor, and tremulous cervical dystonia. Proc Natl Acad Sci USA. 2015;112:E2268. - PMC - PubMed
    1. Louis ED. “Essential tremor” or “the essential tremors”: Is this one disease or a family of diseases? Neuroepidemiology. 2014;42(2):81–89. - PMC - PubMed
    1. Jiménez-Jiménez FJ, et al. Update on genetics of essential tremor. Acta Neurol Scand. 2013;128(6):359–371. - PubMed
    1. McClellan J, King M-C. Genetic heterogeneity in human disease. Cell. 2010;141(2):210–217. - PubMed

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