MeSH Browser

MeSH Supplementary: Phosphoserine Aminotransferase Deficiency
Unique ID: C567032
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567032
Entry Term(s): PSAT Deficiency
Registry Numbers: 0
Heading Mapped to: Transaminases / deficiency; *Microcephaly; *Psychomotor Disorders; *Seizures
Frequency: 5
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Phosphoserine Aminotransferase Deficiency MeSH Supplementary Concept Data 2025