<em>TBC1D24</em> Mutations in a Sibship with Multifocal Polymyoclonus
<p><strong>Background:</strong> 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> A family with two af...
Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Ubiquity Press
2017-04-01
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Series: | Tremor and Other Hyperkinetic Movements |
Online Access: | https://tremorjournal.org/index.php/tremor/article/view/452 |