MeSH Browser

MeSH Supplementary: Spastic Paraplegia 32, Autosomal Recessive
Unique ID: C566983
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566983
Registry Number: 0
Heading Mapped to: *Intellectual Disability; *Spastic Paraplegia, Hereditary
Frequency: 0
Note: also known as SPG32
Date of Entry: 2012/08/24

Spastic Paraplegia 32, Autosomal Recessive MeSH Supplementary Concept Data 2024