Doummar, Diane <br/><br/>
A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Sep 2015 
 - 1431-2 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1531-8257 
<br/><br/><label>Standard No.: </label>10.1002/mds.26303  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carrier Proteins--genetics<br/>Cerebellar Diseases--genetics<br/>Child<br/>Consanguinity<br/>GTPase-Activating Proteins<br/>Humans<br/>Male<br/>Membrane Proteins<br/>Mutation<br/>Myoclonus--genetics<br/>Nerve Tissue Proteins