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Query Trace: Recurrence and ABCC8[original query]

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism. Journal of clinical research in pediatric endocrinology 2015 Dec . Güven Ayla, Cebeci Ay?e Nurcan, Ellard Sian, Flanagan Sarah Similar articles in PubMed
Therapeutic implications of novel mutations of the RFX6 gene associated with early-onset diabetes. The pharmacogenomics journal 2015 Feb 15 (1): 49-54. Artuso R, Provenzano A, Mazzinghi B, Giunti L, Palazzo V, Andreucci E, Blasetti A, Chiuri R M, Gianiorio F E, Mandich P, Monami M, Mannucci E, Giglio Similar articles in PubMed
Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency. Diabetic medicine : a journal of the British Diabetic Association 2013 May 30 (5): e197-200. De Franco E, Shaw-Smith C, Flanagan S E, Edghill E L, Wolf J, Otte V, Ebinger F, Varthakavi P, Vasanthi T, Edvardsson S, Hattersley A T, Ellard Similar articles in PubMed