Turkish Society for Pediatric Endocrinology and Diabetes
ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern Anatolia [J Clin Res Pediatr Endocrinol]
ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern Anatolia
Özlem Sangün1, Bilin Çetinkaya2, Khalid Hussein31Baskent University Faculty Of Medicine, Department Of Pediatric Endocrinology, Ankara, Turkey 2Baskent University Faculty Of Medicine, Department Of Neonatology, Ankara, Turkey\R\N 3Ucl Institute Of Child Health, Clinical And Molecular Genetics Unit, Developmental Endocrinology Research Group, Uk
Özlem Sangün, Bilin Çetinkaya, Khalid Hussein. ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern Anatolia. J Clin Res Pediatr Endocrinol. 2015; 7(1): 20-20 Manuscript Language: English