Associated Papers
Composite Digenic Diabetes Linked to Heterozygous Variants of <italic>GCK</italic> and <italic>NEUROD1</italic>: A Case Report.
Rapini N et al.
Hormone Research in Paediatrics, 2025
Disease-causing mutations in genes encoding transcription factors critical for photoreceptor development.
Sun C et al.
Frontiers in Molecular Neuroscience, 2023
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
NEUROD1 mutation in an Italian patient with maturity onset diabetes of the young 6: a case report.
Brodosi L et al.
Bmc Endocrine Disorders, 2021
Select a paper to view details