The miR-668 binding site variant rs1046322 on WFS1 is associated with obesity in Southeast Asians

The Wolfram syndrome 1 gene (WFS1) is the main causative locus for Wolfram syndrome, an inherited condition characterized by childhood-onset diabetes mellitus, optic atrophy, and deafness. Global genome-wide association studies have listed at least 19 WFS1 variants that are associated with type 2 di...

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Detalles Bibliográficos
Autores principales: Hammad, Maha M., Abu-Farha, Mohamed, Hebbar, Prashantha, Anoop, Emil, Chandy, Betty, Melhem, Motasem, Channanath, Arshad, Al-Mulla, Fahd, Thanaraj, Thangavel Alphonse, Abubaker, Jehad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583568/
https://www.ncbi.nlm.nih.gov/pubmed/37859980
http://dx.doi.org/10.3389/fendo.2023.1185956

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583568/
https://www.ncbi.nlm.nih.gov/pubmed/37859980
http://dx.doi.org/10.3389/fendo.2023.1185956

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