Motor Deficits and Cerebellar Atrophy in Elovl5 Knock Out Mice
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DOI: 10.3389/fncel.2017.00343
Abstract: 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… read more here.
Keywords: elovl5 knock; knock mice; cerebellar atrophy; mice ... See more keywords