Behn, P S <br/><br/>
Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.  [electronic resource] 

 -  Diabetes  Jun 1998 
 - 967-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0012-1797 
<br/><br/><label>Standard No.: </label>10.2337/diabetes.47.6.967  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aged<br/>Aged, 80 and over<br/>DNA--blood<br/>DNA-Binding Proteins--genetics<br/>Diabetes Mellitus, Type 2--genetics<br/>Europe, Eastern--ethnology<br/>Exons<br/>Genetic Variation<br/>Hepatocyte Nuclear Factor 1<br/>Hepatocyte Nuclear Factor 1-alpha<br/>Hepatocyte Nuclear Factor 1-beta<br/>Humans<br/>Israel<br/>Jews--genetics<br/>Middle Aged<br/>Nuclear Proteins<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Transcription Factors--biosynthesis