Effects of the administration of Elovl5-dependent fatty acids on a spino-cerebellar ataxia 38 mouse model
Abstract 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 la...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2022-08-01
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Series: | Behavioral and Brain Functions |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12993-022-00194-4 |