MeSH Browser

MeSH Supplementary: Ataxia, Spastic, 2, Autosomal Recessive
Unique ID: C566969
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566969
Heading Mapped to: Cerebellar Ataxia / congenital; *Spastic Paraplegia, Hereditary
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Ataxia, Spastic, 2, Autosomal Recessive MeSH Supplementary Concept Data 2024