Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia

Clinical Endocrinology,Volume 0, Issue ja, -Not available-.

Source: Clinical Endocrinology - August 23, 2018 Category: Endocrinology Authors: Thomas W Laver , Matthew N Wakeling , Janet Hong Yeow Hua , Jayne AL Houghton , Khalid Hussain , Sian Ellard , Sarah E Flanagan Source Type: research