Rötig, A <br/><br/>
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).  [electronic resource] 

 -  The Journal of clinical investigation  Mar 1993 
 - 1095-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-9738 
<br/><br/><label>Standard No.: </label>10.1172/JCI116267  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Base Sequence<br/>Blotting, Southern<br/>DNA, Mitochondrial--genetics<br/>Electron Transport Complex IV--metabolism<br/>Female<br/>Humans<br/>Lymphocytes--enzymology<br/>Molecular Sequence Data<br/>Muscles--enzymology<br/>NADH Dehydrogenase--metabolism<br/>Oligodeoxyribonucleotides<br/>Sequence Deletion<br/>Succinate Cytochrome c Oxidoreductase--metabolism<br/>Wolfram Syndrome--enzymology