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Title
Motor Deficits and Cerebellar Atrophy in Elovl5 Knock Out Mice
Authors
Keywords
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Journal
Frontiers in Cellular Neuroscience
Volume 11, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2017-10-30
DOI
10.3389/fncel.2017.00343
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- Consensus Paper: Revisiting the Symptoms and Signs of Cerebellar Syndrome
- (2015) Florian Bodranghien et al. CEREBELLUM
- Redefining the cerebellar cortex as an assembly of non-uniform Purkinje cell microcircuits
- (2015) Nadia L. Cerminara et al. NATURE REVIEWS NEUROSCIENCE
- A new humanized ataxin-3 knock-in mouse model combines the genetic features, pathogenesis of neurons and glia and late disease onset of SCA3/MJD
- (2015) Pawel M. Switonski et al. NEUROBIOLOGY OF DISEASE
- A NewELOVL4Mutation in a Case of Spinocerebellar Ataxia With Erythrokeratodermia
- (2015) Cynthia V. Bourassa et al. JAMA Neurology
- A Novel Mutation inELOVL4Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia
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- (2014) Eleonora Di Gregorio et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2014) Roxanne Larivière et al. HUMAN MOLECULAR GENETICS
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- (2014) Maxime Cadieux-Dion et al. JAMA Neurology
- Very long-chain fatty acids: elongation, physiology and related disorders
- (2012) A. Kihara JOURNAL OF BIOCHEMISTRY
- Motor dysfunction and cerebellar Purkinje cell firing impairment in Ebf2 null mice
- (2012) Eriola Hoxha et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Excitability and Synaptic Alterations in the Cerebellum of APP/PS1 Mice
- (2012) Eriola Hoxha et al. PLoS One
- The key roles of elongases and desaturases in mammalian fatty acid metabolism: Insights from transgenic mice
- (2009) Hervé Guillou et al. PROGRESS IN LIPID RESEARCH
- Deletion of ELOVL5 leads to fatty liver through activation of SREBP-1c in mice
- (2008) Young-Ah Moon et al. JOURNAL OF LIPID RESEARCH
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