Juvenile myoclonic epilepsy (JME) is a distinct epileptic syndrome with a complex mode of inheritance. Several studies found evidence for a locus involved in JME on chromosome 6 near the HLA region. Recently, Elmslie et al. [1997] reported evidence of linkage in JME to chromosome 15q14 assuming a re
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1
✍ Scribed by Sander, Thomas ;Windemuth, Christine ;Schulz, Herbert ;Saar, Kathrin ;Gennaro, Elena ;Bianchi, Amedeo ;Zara, Federico ;Bulteau, Christine ;Kaminska, Anna ;Ville, Doroth�e ;Cieuta, C�cile ;Prud'homme, Jean-Fran�ois ;Dulac, Olivier ;Bate, Louise ;Gardiner, R. Mark ;de Haan, Gerrit-Jan ;Janssen, Guus A.M.A.J. ;Witte, Jorine ;Halley, Dicky J.J. ;Lindhout, Dick ;Wienker, Thomas F. ;Janz, Dieter ;,
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 95 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0148-7299
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Juvenile myoclonic epilepsy (JME) is a genetically determined common subtype of idiopathic generalized epilepsy (IGE). Significant evidence for linkage has been reported for a susceptibility locus for JME in the chromosomal region 15q14 that harbors the gene encoding the ␣7 subunit of the neuronal n