par Catarino, Claudia B;Kasperavičiūtė, Dalia;Thom, Maria;Cavalleri, Gianpiero L;Martinian, Lillian;Heinzen, Erin;Dorn, Thomas;Grunwald, Thomas;Chaila, Elijah;Depondt, Chantal ;Krämer, Günter;Delanty, Norman;Goldstein, David B;Sisodiya, Sanjay M
Référence Epilepsia, 52, 8, page (1388-1392)
Publication Publié, 2011-08
Référence Epilepsia, 52, 8, page (1388-1392)
Publication Publié, 2011-08
Article révisé par les pairs
Résumé : | Several recent reports of genomic microdeletions in epilepsy will generate further research; discovery of more microdeletions and other important classes of variants may follow. Detection of such genetic abnormalities in patients being evaluated for surgical treatment might raise concern that a genetic defect, possibly widely expressed in the brain, will affect surgical outcome. |