Rare variants in WFS1 gene in patients with young-onset diabetes
Четырнадцатая международная мультиконференция : Тез. докл.semanticscholar +1 more source
The Valdivia Project: genetic characterization of a unique Wolfram Syndrome cluster in coastal Ecuador. [PDF]
Orphanet J Rare DisPalacio JE +6 more
europepmc +1 more source
Advances in Research on Endoplasmic Reticulum-Associated Degradation Mechanisms in Neurodegenerative Diseases. [PDF]
Cell Mol NeurobiolKong B +8 more
europepmc +1 more source
Erratum. Liraglutide Treatment Reverses Unconventional Cellular Defects in Induced Pluripotent Stem Cell-Derived β-Cells Harboring a Partially Functional WFS1 Variant. Diabetes 2025;74:1273-1288. [PDF]
DiabetesTorchio S +10 more
europepmc +1 more source
Neutropenia Through Enhanced Neutrophil Apoptosis and Secondary Necrosis in Wolfram Syndrome 1 [PDF]
Turk J HaematolAslan D, Kayhan H.
europepmc +1 more source
Proximal 4p deletion syndrome in a woman with intellectual disability: a case report and literature review. [PDF]
Mol CytogenetWei L, He Y, Liu D, Chi X, Qin X.
europepmc +1 more source
Cross-tissue transcriptome-wide association identify novel T1D susceptibility genes and drug candidates. [PDF]
Front ImmunolLiu Y, Cao Y, Jiang Y.
europepmc +1 more source
Diabetes Insipidus as an Early Clinical Indicator of Wolfram Syndrome Type 1: Evidence From a Symptom-Based Screening Approach. [PDF]
Pediatr DiabetesGundogdu Ogutlu OB +5 more
europepmc +1 more source
Pregnancy and Peripartum Multidisciplinary Management in Wolfram Syndrome Type 1: A Case Report. [PDF]
Diagnostics (Basel)Esteban-Bueno G, Serrano Rodríguez ML.
europepmc +1 more source
Targeted analysis of whole exome sequencing in Thai patients with neonatal diabetes. [PDF]
Hum GenetPlengvidhya N +7 more
europepmc +1 more source