Associated Papers
Identification of gene mutations associated with type 1 diabetes by next-generation sequencing in affected Palestinian families.
Bawatneh A et al.
Frontiers in Genetics, 2023
Insights into the Genetics and Signaling Pathways in Maturity-Onset Diabetes of the Young.
Sousa M et al.
International Journal of Molecular Sciences, 2022
The first case of NEUROD1-MODY reported in Latin America.
Abreu GM et al.
Molecular Genetics & Genomic Medicine, 2019
Genetic Dissection and Clinical Features of MODY6 (NEUROD1-MODY).
Horikawa Y et al.
Current Diabetes Reports, 2019
Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene.
Orosz O et al.
Molecular Vision, 2015
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities.
Rubio-Cabezas O et al.
Diabetes, 2010
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