MeSH Browser

MeSH Supplementary: Spastic Paraplegia 44, Autosomal Recessive
Unique ID: C567707
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567707
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 0
Note: also known as SPG44; associated with mutations of GJC2 gene which encodes gap junction protein, gamma-2
Date of Entry: 2012/08/24
Revision Date: 1955/01/01

Spastic Paraplegia 44, Autosomal Recessive MeSH Supplementary Concept Data 2024