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. HORMONE RESEARCH IN PAEDIATRICS , vol.86 , 204-205.

HATİPOĞLU, N., DEMİRBİLEK, H., Gul, U., Tatli, Z. U., Flanagan, S., Ellard, S., ... De Franco, E.(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. HORMONE RESEARCH IN PAEDIATRICS , vol.86, 204-205.

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," HORMONE RESEARCH IN PAEDIATRICS , vol.86, 204-205, 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." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.204-205, 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." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.204-205.

@article{article, 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}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2016, pages={204-205} }