Homozygous Mutations in NEUROD1 Are Responsible for a Novel Syndrome of Permanent Neonatal Diabetes and Neurological Abnormalities

por Rubio-Cabezas, Oscar, Minton, Jayne A.L., Kantor, Iren, Williams, Denise, Ellard, Sian, Hattersley, Andrew T.
Publicado 2010

Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene

por Orosz, Orsolya, Czeglédi, Miklós, Kántor, Irén, Balogh, István, Vajas, Attila, Takács, Lili, Berta, András, Losonczy, Gergely
Publicado 2015

A Comprehensive Analysis of Hungarian MODY Patients—Part I: Gene Panel Sequencing Reveals Pathogenic Mutations in HNF1A, HNF1B, HNF4A, ABCC8 and INS Genes

por Gaál, Zsolt, Szűcs, Zsuzsanna, Kántor, Irén, Luczay, Andrea, Tóth-Heyn, Péter, Benn, Orsolya, Felszeghy, Enikő, Karádi, Zsuzsanna, Madar, László, Balogh, István
Publicado 2021

A Comprehensive Analysis of Hungarian MODY Patients—Part II: Glucokinase MODY Is the Most Prevalent Subtype Responsible for about 70% of Confirmed Cases

por Gaál, Zsolt, Szűcs, Zsuzsanna, Kántor, Irén, Luczay, Andrea, Tóth-Heyn, Péter, Benn, Orsolya, Felszeghy, Enikő, Karádi, Zsuzsanna, Madar, László, Balogh, István
Publicado 2021