Schwartz, Faina <br/><br/>
Mitochondrial genome mutations in hypertensive individuals.  [electronic resource] 

 -  American journal of hypertension  Jul 2004 
 - 629-35 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0895-7061 
<br/><br/><label>Standard No.: </label>10.1016/j.amjhyper.2004.02.020  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Black People--genetics<br/>Boston<br/>DNA Mutational Analysis<br/>DNA, Mitochondrial--genetics<br/>Family Health<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Variation--genetics<br/>Genome, Human<br/>Greece<br/>Humans<br/>Hypertension--genetics<br/>Open Reading Frames--genetics<br/>Pedigree<br/>Point Mutation--genetics<br/>Polymorphism, Genetic--genetics<br/>RNA, Ribosomal--genetics<br/>RNA, Transfer--genetics<br/>Sequence Analysis, DNA<br/>White People--genetics<br/>Black or African American