Watts, Giles D J <br/><br/>
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.  [electronic resource] 

 -  Nature genetics  Apr 2004 
 - 377-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng1332  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases<br/>Cell Cycle Proteins--genetics<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 9<br/>Female<br/>Humans<br/>Immunohistochemistry<br/>Male<br/>Muscular Diseases--genetics<br/>Mutation<br/>Osteitis Deformans--genetics<br/>Pedigree<br/>Valosin Containing Protein