MeSH Browser

MeSH Supplementary: Striatal Degeneration, Autosomal Dominant
Unique ID: C563783
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563783
Registry Number: 0
Heading Mapped to: Corpus Striatum / *pathology; Nerve Degeneration / *congenital
Frequency: 4
Note: mutation in PDE8B
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Striatal Degeneration, Autosomal Dominant MeSH Supplementary Concept Data 2024