MeSH Browser

MeSH Supplementary: Spastic Paraplegia 33, Autosomal Dominant
Unique ID: C565214
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565214
Registry Number: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 0
Note: also known as SPG33; associated with mutations in ZFYVE27, the gene for zinc finger FYVE domain-containing protein 27
Date of Entry: 2012/08/24

Spastic Paraplegia 33, Autosomal Dominant MeSH Supplementary Concept Data 2023