Yorifuji, Tohru <br/><br/>
Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  Jan 2011 
 - E141-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1945-7197 
<br/><br/><label>Standard No.: </label>10.1210/jc.2010-1281  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Asian People--genetics<br/>Congenital Hyperinsulinism--genetics<br/>DNA Mutational Analysis<br/>Humans<br/>Infant<br/>KATP Channels--genetics<br/>Microdissection<br/>Mutation<br/>Pancreatectomy