Motor Deficits and Cerebellar Atrophy in Elovl5 Knock Out Mice

Spino-Cerebellar-Ataxia type 38 (SCA38) is caused by missense mutations in the very long chain fatty acid elongase 5 gene, ELOVL5. The main clinical findings in this disease are ataxia, hyposmia and cerebellar atrophy. Mice in which Elovl5 has been knocked out represent a model of the loss of functi...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670146/
https://www.ncbi.nlm.nih.gov/pubmed/29163054
http://dx.doi.org/10.3389/fncel.2017.00343

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670146/
https://www.ncbi.nlm.nih.gov/pubmed/29163054
http://dx.doi.org/10.3389/fncel.2017.00343

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