May, D L <br/><br/>
Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease.  [electronic resource] 

 -  Archives of neurology  Sep 1968 
 - 331-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.1968.00480030109013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Cerebellar Ataxia--genetics<br/>Cerebral Cortex--physiopathology<br/>Deafness--genetics<br/>Electroencephalography<br/>Female<br/>Humans<br/>Light<br/>Male<br/>Middle Aged<br/>Muscles--physiopathology<br/>Myoclonus--classification<br/>Pedigree