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Effects of the administration of Elovl5-dependent fatty acids on a spino-cerebellar ataxia 38 mouse model
BACKGROUND: Spinocerebellar ataxia 38 (SCA38) is a rare autosomal neurological disorder characterized by ataxia and cerebellar atrophy. SCA38 is caused by mutations of ELOVL5 gene. ELOVL5 gene encodes a protein, which elongates long chain polyunsaturated fatty acids (PUFAs). Knockout mice lacking El...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9357323/ https://www.ncbi.nlm.nih.gov/pubmed/35933444 http://dx.doi.org/10.1186/s12993-022-00194-4 |