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Human Disease

autosomal recessive spinocerebellar ataxia 28

Term ID
DOID:0070409
Synonyms
  • 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 )
Relationships
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Genes Involved
Zebrafish Models