Open AccessEPILEPSY CAUSED BY PCDH19 GENE MUTATION: A REVIEW OF LITERATURE AND THE AUTHORS’ OBSERVATIONS
Author(s) -
К. Ю. Мухин,
О. А. Пылаева,
А. Ф. Долинина,
Svetlana Moiseeva,
Ю. В. Вербицкая,
А. С. Петрухин,
Г. Клюгер,
Х. Хольтхаузен,
М. Штаудт
Publication year - 2016
Publication title -
russkij žurnal detskoj nevrologii
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.139
H-Index - 2
eISSN - 2412-9178
pISSN - 2073-8803
DOI - 10.17650/2073-8803-2016-11-2-26-32
Subject(s) - levetiracetam , dravet syndrome , epilepsy , valproic acid , medicine , topiramate , pediatrics , genetic testing , oxcarbazepine , mutation , status epilepticus , phenobarbital , intellectual disability , gene mutation , carbamazepine , psychiatry , genetics , gene , biology