Dotto, Renata P <br/><br/>
Unexpected finding of a whole HNF1B gene deletion during the screening of rare MODY types in a series of Brazilian patients negative for GCK and HNF1A mutations.  [electronic resource] 

 -  Diabetes research and clinical practice  Jun 2016 
 - 100-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1872-8227 
<br/><br/><label>Standard No.: </label>10.1016/j.diabres.2016.04.035  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Brazil<br/>Case-Control Studies<br/>Central Nervous System Diseases<br/>Dental Enamel--abnormalities<br/>Diabetes Mellitus, Type 2--diagnosis<br/>Female<br/>Gene Deletion<br/>Glucokinase--genetics<br/>Hepatocyte Nuclear Factor 1-alpha--genetics<br/>Hepatocyte Nuclear Factor 1-beta--genetics<br/>Heterozygote<br/>Humans<br/>Incidental Findings<br/>Kidney Diseases, Cystic<br/>Male<br/>Phenotype