Deafness, Congenital, and Familial Myoclonic Epilepsy MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Deafness, Congenital, and Familial Myoclonic Epilepsy
Unique ID: C565649
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565649
Registry Number: 0
Heading Mapped to: Deafness / *congenital; *Epilepsies, Myoclonic
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Deafness, Congenital, and Familial Myoclonic Epilepsy Preferred

page delivered in 0.005s