HATİPOĞLU, N. Et Al. 2016. 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. 55 th Annual ESPE meeting .

HATİPOĞLU, N., DEMİRBİLEK, H., GÜL, Ü., UZAN TATLI, Z., FALANAGAN, S., ELLARD, S., ... ELİSA DE, F.(2016). 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 . 55 th Annual ESPE meeting

HATİPOĞLU, NİHAL Et Al. "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," 55 th Annual ESPE meeting, 2016

HATİPOĞLU, NİHAL Et Al. "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." 55 th Annual ESPE meeting , 2016

HATİPOĞLU, N. Et Al. (2016) . "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." 55 th Annual ESPE meeting .

@conferencepaper{conferencepaper, author={NİHAL HATİPOĞLU Et Al. }, title={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}, congress name={55 th Annual ESPE meeting}, city={}, country={}, year={2016}}