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LINGO1 variants in essential tremor and Parkinson's disease.

Identifieur interne : 000073 ( PubMed/Corpus ); précédent : 000072; suivant : 000074

LINGO1 variants in essential tremor and Parkinson's disease.

Auteurs : H. Deng ; S. Gu ; J. Jankovic

Source :

RBID : pubmed:21470193

English descriptors

Abstract

The leucine-rich repeat and Ig domain containing 1 gene (LINGO1), recently considered to be conferred increased risk of essential tremor (ET), has been also implicated in Parkinson disease (PD). As the two common movement disorders have overlapping clinical and pathological features, it has been postulated that the LINGO1 gene may play a role in the pathogenesis of the two diseases. Here, we review published reports of the LINGO1 variants in ET and PD in an attempt to better understand the molecular and pathogenic relationship of LINGO1 to the two disorders.

DOI: 10.1111/j.1600-0404.2011.01516.x
PubMed: 21470193

Links to Exploration step

pubmed:21470193

Le document en format XML

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<div type="abstract" xml:lang="en">The leucine-rich repeat and Ig domain containing 1 gene (LINGO1), recently considered to be conferred increased risk of essential tremor (ET), has been also implicated in Parkinson disease (PD). As the two common movement disorders have overlapping clinical and pathological features, it has been postulated that the LINGO1 gene may play a role in the pathogenesis of the two diseases. Here, we review published reports of the LINGO1 variants in ET and PD in an attempt to better understand the molecular and pathogenic relationship of LINGO1 to the two disorders.</div>
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