Two Cases of Unverricht-Lundborg Disease with Mutation in the Gene Encoding Cystatin B
Open Access
- 1 January 1998
- journal article
- Published by The Japan Epilepsy Society in Journal of the Japan Epilepsy Society
- Vol. 16 (2) , 100-108
- https://doi.org/10.3805/jjes.16.100
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- PROGRESSIVE MYOCLONUS EPILEPSYActa Neurologica Scandinavica, 2009
- PROGRESSIVE MYOCLONUS EPILEPSYActa Neurologica Scandinavica, 2009
- NEUROPATHOLOGICAL STUDIES IN THREE SCANDINAVIAN CASES OF PROGRESSIVE MYOCLONUS EPILEPSYActa Neurologica Scandinavica, 2009
- MYOCLONUS EPILEPSY (UNVERRICHT-LUNDBORG) IN FINLANDActa Neurologica Scandinavica, 2009
- Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1Nature Genetics, 1997
- Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsyNature, 1997
- Unstable insertion in the 5′ flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1Nature Genetics, 1997
- Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)Science, 1996
- "BALTIC" MYOCLONUS EPILEPSY: HEREDITARY DISORDER OF CHILDHOOD MADE WORSE BY PHENYTOINThe Lancet, 1983
- Progressive myoclonus epilepsy: genetic and nosological aspects with special reference to 107 Finnish patientsClinical Genetics, 1979