Whole Exome Sequencing in Children With Type 1 Diabetes Before Age 6 Years Reveals Insights Into Disease Heterogeneity
Conclusions: WES found potentially deleterious rare variants in MODY genes in 8.1% of EOT1D, occurring in the context of a T1D genetic background. Such genetic variants may contribute to disease precipitation by a β-cell dysfunction mechanism. This supports the concept of different endotypes of T1D,...
Saved in:
| Main Authors: | Andreia Fiúza Ribeiro, Ana Laura Fitas, Marcela Oliveira Pires, Paula Matoso, Dário Ligeiro, Daniel Sobral, Carlos Penha-Gonçalves, Jocelyne Demengeot, Íris Caramalho, Catarina Limbert |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2024-01-01
|
| Series: | Journal of Diabetes Research |
| Online Access: | http://dx.doi.org/10.1155/2024/3076895 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Whole Exome Sequencing in Atrial Fibrillation.
by: Steven A Lubitz, et al.
Published: (2016-09-01) -
Whole-exome sequencing of patients with juvenile myoclonic epilepsy
by: E. E. Timechko, et al.
Published: (2022-10-01) -
Whole Exome Sequencing in Chinese Pediatric Patients With Nephrolithiasis
by: Xiaochuan Wang, et al.
Published: (2025-08-01) -
Whole exome sequencing enhances diagnosis of hereditary bronchiectasis
by: Wangji Zhou, et al.
Published: (2025-03-01) -
Whole-exome sequencing analysis identifies risk genes for schizophrenia
by: Sophie L. Chick, et al.
Published: (2025-08-01)