Lehto, M <br/><br/>
High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes.  [electronic resource] 

 -  Diabetologia  Sep 1999 
 - 1131-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0012-186X 
<br/><br/><label>Standard No.: </label>10.1007/s001250051281  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age Factors<br/>Aged<br/>Aged, 80 and over<br/>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors<br/>DNA, Mitochondrial--genetics<br/>DNA-Binding Proteins--genetics<br/>Diabetes Mellitus, Type 2--enzymology<br/>Exons<br/>Family<br/>Female<br/>Genetic Variation<br/>Glucokinase--genetics<br/>Hepatocyte Nuclear Factor 1<br/>Hepatocyte Nuclear Factor 1-alpha<br/>Hepatocyte Nuclear Factor 1-beta<br/>Hepatocyte Nuclear Factor 4<br/>Humans<br/>Introns<br/>Male<br/>Middle Aged<br/>Mutation<br/>Nuclear Proteins<br/>Pedigree<br/>Phosphoproteins--genetics<br/>Point Mutation<br/>Polymorphism, Single-Stranded Conformational<br/>Promoter Regions, Genetic<br/>Scandinavian and Nordic Countries<br/>Sequence Deletion<br/>Transcription Factors--genetics