Towards the identification of a genetic basis for <scp>L</scp>andau‐<scp>K</scp>leffner <scp>s</scp>yndrome

Abstract

A single mutation was identified in the GRIN2A gene. This study has identified a number of additional candidate genes including RELN, BSN, EPHB2, and NID2. A PowerPoint slide summarizing this article is available for download in the Supporting Information section here.