A variant in the <i>HS1-BP3</i> gene is associated with familial essential tremor

200580 citationsJournal Articlegreen Open Access

Authors

J. J. Higgins · Parkinson's and Movement Disorder Institute

Raffaella Lombardi · Parkinson's and Movement Disorder Institute

Joanna Pucilowska · Parkinson's and Movement Disorder Institute

Joseph Jankovic · Parkinson's and Movement Disorder Institute

Ek Khoon Tan · Parkinson's and Movement Disorder Institute

John P. Rooney · Parkinson's and Movement Disorder Institute

Abstract

A rare variant in the HS1-BP3 gene that is associated with essential tremor (ET) in two families is reported. This finding will facilitate research on the functional role of this gene and related genes in the pathogenesis of ET.

Topics & Keywords

Neurological disorders and treatments Genetics and Neurodevelopmental Disorders Glycogen Storage Diseases and Myoclonus

Publication Details

Published in: Neurology

Volume 64, Issue 3, pp. 417-421

DOI: 10.1212/01.wnl.0000153481.30222.38

Field-Weighted Citation Impact: 6.90

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A variant in the <i>HS1-BP3</i> gene is associated with familial essential tremor

Authors

Abstract

Topics & Keywords

Publication Details