Watts, G D J <br/><br/>
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.  [electronic resource] 

 -  Clinical genetics  Nov 2007 
 - 420-6 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>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2007.00887.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Adult<br/>Cell Cycle Proteins--genetics<br/>DNA Mutational Analysis<br/>Dementia--complications<br/>Female<br/>Humans<br/>Male<br/>Middle Aged<br/>Models, Molecular<br/>Mutation<br/>Myositis, Inclusion Body--complications<br/>Osteitis Deformans--complications<br/>Pedigree<br/>Valosin Containing Protein