Al-Obeidi, E <br/><br/>
Genotype-phenotype study in patients with valosin-containing protein mutations associated with multisystem proteinopathy.  [electronic resource] 

 -  Clinical genetics  Jan 2018 
 - 119-125 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.13095  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aged<br/>Alzheimer Disease--genetics<br/>Amyotrophic Lateral Sclerosis--genetics<br/>Cohort Studies<br/>Family Health<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Genotype<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Parkinson Disease--genetics<br/>Phenotype<br/>Valosin Containing Protein--genetics<br/>Young Adult