Fischel-Ghodsian, N <br/><br/>
Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders.  [electronic resource] 

 -  Molecular genetics and metabolism   
 - 93-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review 
<br/><br/><label>ISSN: </label>1096-7192 
<br/><br/><label>Standard No.: </label>10.1006/mgme.2000.3014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA, Mitochondrial--genetics<br/>Humans<br/>Mitochondrial Myopathies--etiology<br/>Mutation<br/>Organ Specificity<br/>Phenotype<br/>Presbycusis--etiology