Maassen, J A <br/><br/>
A case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness.  [electronic resource] 

 -  Archives of physiology and biochemistry  Jul 2002 
 - 186-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1381-3455 
<br/><br/><label>Standard No.: </label>10.1076/apab.110.3.186.8294  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA, Mitochondrial<br/>Deafness--genetics<br/>Diabetes Mellitus--genetics<br/>Female<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Syndrome