MeSH Browser

MeSH Supplementary: Amish Infantile Epilepsy Syndrome
Unique ID: C563799
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563799
Entry Term(s): Epilepsy Syndrome, Infantile-Onset Symptomatic; GM3 Synthase Deficiency
Registry Numbers: 0
Heading Mapped to: *Epilepsy; Sialyltransferases / deficiency
Frequency: 14
Note: mutation in GM3 synthetase
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Amish Infantile Epilepsy Syndrome MeSH Supplementary Concept Data 2025