Mastaglia, F L <br/><br/>
Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Dec 2013 
 - 969-74 p.  digital 
<br/><br/> Publication Type: 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.2013.09.008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Aged<br/>Apolipoproteins E--genetics<br/>Female<br/>Gene Frequency<br/>Genetic Predisposition to Disease--genetics<br/>Genotype<br/>Humans<br/>Kaplan-Meier Estimate<br/>Male<br/>Membrane Transport Proteins--genetics<br/>Middle Aged<br/>Mitochondrial Precursor Protein Import Complex Proteins<br/>Myositis, Inclusion Body--genetics<br/>Polymorphism, Single Nucleotide--genetics<br/>Trinucleotide Repeat Expansion--genetics