Previtali, Stefano C <br/><br/>
Expanding the central nervous system disease spectrum associated with FLNC mutation.  [electronic resource] 

 -  Muscle & nerve  05 2019 
 - E33-E37 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1097-4598 
<br/><br/><label>Standard No.: </label>10.1002/mus.26443  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Ataxia<br/>Atrophy<br/>Cerebellar Ataxia--diagnostic imaging<br/>Cerebellum--diagnostic imaging<br/>Female<br/>Filamins--genetics<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Muscle, Skeletal--pathology<br/>Myopathies, Structural, Congenital--diagnostic imaging<br/>Pedigree<br/>Siblings<br/>Spinal Cord--diagnostic imaging