MeSH Browser

MeSH Supplementary: Spinocerebellar Ataxia 31
Unique ID: C566146
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566146
Entry Term(s): SCA31 Spinocerebellar Ataxia 31; Spinocerebellar Ataxia, 16q22-Linked
Registry Numbers: 0
Heading Mapped to: *Spinocerebellar Ataxias
Frequency: 16
Note: caused by a 2.5- to 3.8-kb insertion containing pentanucleotide repeats including (TGGAA)n within an intron of the BEAN gene on chromosome 16q21-q22.
Date of Entry: 2012/11/05
Revision Date: 2019/06/24

Spinocerebellar Ataxia 31 MeSH Supplementary Concept Data 2024