Associated Papers
Identification of candidate gene variants of monogenic diabetes using targeted panel sequencing in early onset diabetes patients.
Lee DH et al.
Bmj Open Diabetes Research & Care, 2021
Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8.
Mouron-Hryciuk J et al.
Annals of Pediatric Endocrinology & Metabolism, 2021
Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations.
Arya VB et al.
European Journal of Endocrinology, 2014
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.
Kapoor RR et al.
European Journal of Endocrinology, 2013
23345197 (PubMed )
Supplement: supp_EJE-12-0673_EJE_120673_Suppl_Table.pdf
Select a paper to view details