Mutations of DEPDC5 for diagnosing epilepsic diseases, disorders or conditions

摘要

The present invention relates to a method for diagnosing an epileptic disease, disorder or condition in a subject, or determining a predisposition of a subject to an epileptic disease, disorder or condition or determining an increased risk of a subject of developing an epileptic disease, disorder or condition, wherein said method comprises determining the status of the DEPDC5 gene of the subject.