A Syndrome of Permanent Neonatal Diabetes Mellitus and Neurological Abnormalities due to a Novel Homozygous Missense c 449T A p I150N Mutation in NEUROD1 Gene

HATİPOĞLU N. , DEMİRBİLEK H., GÜL Ü. , UZAN TATLI Z. , FALANAGAN S., ELLARD S., ...Daha Fazla

55 th Annual ESPE meeting, 10 Eylül 2016