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

 -  Journal of inherited metabolic disease  1993 
 - 527-30 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1007/BF00711672  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Blotting, Southern<br/>DNA Probes<br/>DNA, Mitochondrial--genetics<br/>Female<br/>Humans<br/>Infant<br/>Lactates--metabolism<br/>Mitochondria, Muscle--genetics<br/>Molecular Sequence Data<br/>Polymerase Chain Reaction<br/>Pyruvates--metabolism<br/>Sequence Deletion<br/>Wolfram Syndrome--genetics