van Essen, E H <br/><br/>
HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.  [electronic resource] 

 -  Diabetic medicine : a journal of the British Diabetic Association  Dec 2000 
 - 841-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0742-3071 
<br/><br/><label>Standard No.: </label>10.1046/j.1464-5491.2000.00379.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>DNA Mutational Analysis<br/>DNA, Mitochondrial--genetics<br/>Deafness--complications<br/>Diabetes Complications<br/>Diabetes Mellitus--genetics<br/>Diabetes Mellitus, Type 1--genetics<br/>Diabetes Mellitus, Type 2--genetics<br/>Genetic Carrier Screening<br/>HLA-DQ Antigens--genetics<br/>HLA-DQ alpha-Chains<br/>HLA-DQ beta-Chains<br/>Humans<br/>Leukocytes--chemistry<br/>Middle Aged<br/>Mouth Mucosa--chemistry<br/>Mutation<br/>Phenotype<br/>Polymorphism, Genetic