<em>TBC1D24</em> Mutations in a Sibship with Multifocal Polymyoclonus

<p><strong>Background:</strong>&nbsp;Advances in molecular genetic technologies have improved our understanding of genetic causes of rare neurological disorders with features of myoclonus.</p><p><strong>Case Report:</strong>&nbsp;A family with two af...

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Bibliographic Details
Main Authors: Adeline Ngoh, Jose Bras, Rita Guerreiro, Amy McTague, Joanne Ng, Esther Meyer, W. Kling Chong, Stewart Boyd, Linda MacLellan, Martin Kirkpatrick, Manju A. Kurian
Format: Article
Language:English
Published: Ubiquity Press 2017-04-01
Series:Tremor and Other Hyperkinetic Movements
Online Access:https://tremorjournal.org/index.php/tremor/article/view/452