Guillausseau, P J <br/><br/>
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).  [electronic resource] 

 -  Diabetes & metabolism  04 2004 
 - 181-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study 
<br/><br/><label>ISSN: </label>1262-3636 
<br/><br/><label>Standard No.: </label>10.1016/s1262-3636(07)70105-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Body Height<br/>Body Mass Index<br/>Body Weight<br/>DNA, Mitochondrial--genetics<br/>Deafness--complications<br/>Diabetes Mellitus, Type 1--complications<br/>Diabetic Ketoacidosis--genetics<br/>Female<br/>France<br/>Humans<br/>Male<br/>Middle Aged<br/>Mothers<br/>Mutation--genetics<br/>Sex Ratio