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Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management.\n                      J Clin Res Pediatr Endocrinol\n                      . 2012;4:169\u201381.","DOI":"10.4274\/Jcrpe.821"},{"key":"ref2","doi-asserted-by":"crossref","unstructured":"Demirbilek H, Hussain K. Congenital hyperinsulinism: diagnosis and treatment update.\n                      J Clin Res Pediatr Endocrinol\n                      . 2017;9(Suppl. 2):69\u201387.","DOI":"10.4274\/jcrpe.2017.S007"},{"key":"ref3","doi-asserted-by":"crossref","unstructured":"Gunay-Aygun M, Tuchman M, Font-Montgomery E, et al. PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic disease and congenital hepatic fibrosis.\n                      Mol Genet Metab\n                      . 2010;99:160\u201373.","DOI":"10.1016\/j.ymgme.2009.10.010"},{"key":"ref4","unstructured":"Sweeney WE, Avner ED. Polycystic Kidney Disease, Autosomal Recessive. 2001 July 19 [Updated 2019 Feb 14]. 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