https://pubmed.ncbi.nlm.nih.gov/25065913/
ELOVL5 mutations cause spinocerebellar ataxia 38
Spinocerebellar ataxias (SCAs) are a heterogeneous group of autosomal-dominant neurodegenerative disorders involving the cerebellum and 23 different genes. We...
spinocerebellar ataxiamutationscause
https://www.frontiersin.org/journals/cellular-neuroscience/articles/10.3389/fncel.2017.00343/full
Frontiers | 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...
knock outfrontiersmotordeficits