Shigemoto, M <br/><br/>
Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus.  [electronic resource] 

 -  Internal medicine (Tokyo, Japan)  Mar 1998 
 - 265-72 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0918-2918 
<br/><br/><label>Standard No.: </label>10.2169/internalmedicine.37.265  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Blood Glucose--metabolism<br/>DNA Primers--chemistry<br/>DNA, Mitochondrial--genetics<br/>Diabetes Complications<br/>Diabetes Mellitus--blood<br/>Female<br/>Genotype<br/>Glucose Clamp Technique<br/>Humans<br/>Hypoparathyroidism--blood<br/>Insulin--blood<br/>Insulin Secretion<br/>Male<br/>Middle Aged<br/>Parathyroid Hormone--blood<br/>Pedigree<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>RNA, Transfer, Leu--genetics