MeSH Browser

MeSH Supplementary: Spinocerebellar ataxia 27
Unique ID: C537204
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537204
Entry Term(s): Cerebellar ataxia, autosomal dominant, FGF14-related; SCA27 Spinocerebellar ataxia 27
Registry Number: 0
Heading Mapped to: *Spinocerebellar Degenerations
Frequency: 10
Date of Entry: 2010/08/25
Revision Date: 2019/06/24

Spinocerebellar ataxia 27 MeSH Supplementary Concept Data 2023