de Wit, H M <br/><br/>
MIDD or MELAS : that's not the question MIDD evolving into MELAS : a severe phenotype of the m.3243A>G mutation due to paternal co-inheritance of type 2 diabetes and a high heteroplasmy level.  [electronic resource] 

 -  The Netherlands journal of medicine  Dec 2012 
 - 460-2 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1872-9061 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA, Mitochondrial--genetics<br/>Deafness--diagnosis<br/>Diabetes Mellitus, Type 2--diagnosis<br/>Fathers<br/>Genetic Predisposition to Disease<br/>Humans<br/>MELAS Syndrome--diagnosis<br/>Male<br/>Mitochondrial Diseases<br/>Phenotype<br/>Point Mutation