MeSH Browser

MeSH Supplementary: Hypomyelination, Global Cerebral
Unique ID: C567847
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567847
Entry Term(s): AGC1 Deficiency; Aspartate-Glutamate Carrier 1 Deficiency
Heading Mapped to: *Psychomotor Disorders; Antiporters / deficiency; *Hereditary Central Nervous System Demyelinating Diseases; Amino Acid Transport Systems, Acidic / deficiency; *Mitochondrial Diseases
Frequency: 21
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Hypomyelination, Global Cerebral MeSH Supplementary Concept Data 2024