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Congenital Hyperinsulinism And Evolution To Sulfonylurearesponsive Diabetes Later In Life Due To A Novel Homozygous P.L171F Abcc8 Mutation
Işık, Emregül; Demirbilek, Hüseyin; Houghton, Jayne A.; Ellard, Sian; Flanagan, Sarah E.; Hussain, Khalid (2019)Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycemia in infants and children. Recessive inactivating mutations in the ABCC8 and KCNJ11 genes account for approximately 50% of all CHI cases. ...