Search Ontology:
Human Disease
autosomal recessive spinocerebellar ataxia 28
- Term ID
- DOID:0070409
- Synonyms
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- SCAR28
- Definition
- An autosomal recessive cerebellar ataxia characterized by onset in early childhood of mildly delayed motor development, gait ataxia, incoordination of fine motor movements, and dysarthria that has_material_basis_in homozygous mutation in the THG1L gene on chromosome 5q33. https://pubmed.ncbi.nlm.nih.gov/31168944/
- References
- Ontology
- Human Disease ( DOID:0070409 )
- is a type of
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Genes Involved
Zebrafish Models