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
โฆ LIBER โฆ
BRD2 (RING3) Is a Probable Major Susceptibility Gene for Common Juvenile Myoclonic Epilepsy
โ Scribed by Deb K. Pal; Oleg V. Evgrafov; Paula Tabares; Fengli Zhang; Martina Durner; David A. Greenberg
- Book ID
- 117854262
- Publisher
- American Society of Human Genetics
- Year
- 2003
- Tongue
- English
- Weight
- 469 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/377006
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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 โฃ7 subunit of the neuronal n