Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor-Reference-Cited by-同舟云学术

Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

Published:2012-08 Issue:2 Volume:91 Page:313-319
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Merner Nancy D.,Girard Simon L.,Catoire Hélène,Bourassa Cynthia V.,Belzil Véronique V.,Rivière Jean-Baptiste,Hince Pascale,Levert Annie,Dionne-Laporte Alexandre,Spiegelman Dan,Noreau Anne,Diab Sabrina,Szuto Anna,Fournier Hélène,Raelson John,Belouchi Majid,Panisset Michel,Cossette Patrick,Dupré Nicolas,Bernard Geneviève,Chouinard Sylvain,Dion Patrick A.,Rouleau Guy A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference38 articles.

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4. Common misdiagnosis of a common neurological disorder: How are we misdiagnosing essential tremor?;Jain;Arch. Neurol.,2006

5. Essential tremor: An overdiagnosed condition?;Schrag;J. Neurol.,2000

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1. Clinical and genetic features of dominant Essential Tremor in Tuscany, Italy: FUS, CAMTA1, ATXN1 and beyond;Journal of the Neurological Sciences;2024-05

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3. FUS G559A Mutation in a Patient with a Frontotemporal Dementia-Motor Neuron Disease Compatible Syndrome: A Case Report;Journal of Alzheimer's Disease Reports;2023-10-09

4. Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations;Disease Models & Mechanisms;2023-10-01

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