MeSH Browser

MeSH Supplementary: Glutamine deficiency, congenital
Unique ID: C536832
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536832
Entry Term(s): Glutamine synthase deficiency, congenital systemic; Glutamine synthetase deficiency, congenital systemic
Registry Number: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; Glutamate-Ammonia Ligase / *deficiency
Frequency: 6
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Glutamine deficiency, congenital MeSH Supplementary Concept Data 2024