Betts, J <br/><br/>
Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutation.  [electronic resource] 

 -  Neurology  Apr 2008 
 - 1290-2 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000308940.38092.74  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenine--metabolism<br/>Adult<br/>Base Sequence--genetics<br/>DNA Mutational Analysis<br/>DNA, Mitochondrial--genetics<br/>Electron Transport Complex IV--genetics<br/>Energy Metabolism--genetics<br/>Fatal Outcome<br/>Female<br/>Gastrointestinal Diseases--genetics<br/>Gastrointestinal Motility--genetics<br/>Gastrointestinal Tract--metabolism<br/>Genetic Markers--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Guanine--metabolism<br/>Humans<br/>MELAS Syndrome--genetics<br/>Middle Aged<br/>Mitochondria--genetics<br/>Mitochondrial Diseases--genetics<br/>Myocytes, Smooth Muscle--metabolism<br/>Point Mutation--genetics