Motor Deficits and Cerebellar Atrophy in Elovl5 Knock Out Mice-Reference-Cited by-同舟云学术

Motor Deficits and Cerebellar Atrophy in Elovl5 Knock Out Mice

Published:2017-10-30 Issue: Volume:11 Page:
ISSN:1662-5102
Container-title:Frontiers in Cellular Neuroscience
language:
Short-container-title:Front. Cell. Neurosci.

Author:

Hoxha Eriola,Gabriele Rebecca M. C.,Balbo Ilaria,Ravera Francesco,Masante Linda,Zambelli Vanessa,Albergo Cristian,Mitro Nico,Caruso Donatella,Di Gregorio Eleonora,Brusco Alfredo,Borroni Barbara,Tempia Filippo

Funder

Fondazione Telethon

Universitàdegli Studi di Torino

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience

Reference20 articles.

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3. Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38);Borroni;Parkinsonism Relat. Disord.,2016

4. A new ELOVL4 mutation in a case of spinocerebellar ataxia with erythrokeratodermia;Bourassa;JAMA Neurol.,2015

5. Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia;Cadieux-Dion;JAMA Neurol.,2014

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