Sang, Yanmei <br/><br/>
Mutational analysis of ABCC8, KCNJ11, GLUD1, HNF4A and GCK genes in 30 Chinese patients with congenital hyperinsulinism.  [electronic resource] 

 -  Endocrine journal  2014 
 - 901-10 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1348-4540 
<br/><br/><label>Standard No.: </label>10.1507/endocrj.ej13-0398  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People--genetics<br/>Child, Preschool<br/>Cohort Studies<br/>Congenital Hyperinsulinism--genetics<br/>DNA Mutational Analysis<br/>Fathers<br/>Female<br/>Glucokinase--genetics<br/>Glutamate Dehydrogenase--genetics<br/>Hepatocyte Nuclear Factor 4--genetics<br/>Heterozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Potassium Channels, Inwardly Rectifying--genetics<br/>Sulfonylurea Receptors--genetics