Fragile X Mutations and Epilepsy
Abstract
A posiible link between predisposition for epilepsy and mutations in the fragile X mental retardation-1 gene (FMR) was investigated in the Neuropediatric Department, Behandlungszentrum Vogtareuth; and Laboratory of Genetic Diagnostics, Munchen, Germany.
DOI: https://doi.org/10.15844/pedneurbriefs-11-1-6 | Journal eISSN: 2166-6482
Language: English
Page range: 4 - 4
Published on: Jan 1, 1997
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 1997 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.