Al-Tahan, Sejad <br/><br/>
Novel valosin-containing protein mutations associated with multisystem proteinopathy.  [electronic resource] 

 -  Neuromuscular disorders : NMD  06 2018 
 - 491-501 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1873-2364 
<br/><br/><label>Standard No.: </label>10.1016/j.nmd.2018.04.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Amyotrophic Lateral Sclerosis--genetics<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Middle Aged<br/>Muscular Diseases--genetics<br/>Mutation, Missense<br/>Osteitis Deformans--genetics<br/>Parkinson Disease--genetics<br/>Pedigree<br/>Valosin Containing Protein--genetics