Dubois-Laforgue, D <br/><br/>
Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM.  [electronic resource] 

 -  Diabetes care  Aug 1998 
 - 1371-2 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>0149-5992 
<br/><br/><label>Standard No.: </label>10.2337/diacare.21.8.1371  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Aspartic Acid<br/>Cysteine<br/>Diabetes Mellitus, Type 2--genetics<br/>HLA Antigens--genetics<br/>Hemochromatosis--genetics<br/>Hemochromatosis Protein<br/>Histidine<br/>Histocompatibility Antigens Class I--genetics<br/>Homozygote<br/>Humans<br/>Major Histocompatibility Complex<br/>Membrane Proteins<br/>Point Mutation<br/>Reference Values<br/>Tyrosine