Amaratunga, Shenali Anne <br/><br/>
Congenital Hyperinsulinism Caused by Novel Homozygous KATP Channel Gene Variants May Be Linked to Unexplained Neonatal Deaths among Kurdish Consanguineous Families.  [electronic resource] 

 -  Hormone research in paediatrics  2020 
 - 58-65 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1663-2826 
<br/><br/><label>Standard No.: </label>10.1159/000506476  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blood Glucose<br/>Child<br/>Child, Preschool<br/>Congenital Hyperinsulinism--blood<br/>Consanguinity<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Insulin--blood<br/>KATP Channels--genetics<br/>Octreotide--therapeutic use<br/>Pedigree<br/>Perinatal Death