WFS1 gene

This paper provides a review on some of the significant research work done on wearable flexible sensors (WFSs). Sensors… Expand

Person re-identification in a non-overlapping multicamera scenario is an open challenge in computer vision because of the large… Expand

Abstract The adoption of more sustainable behaviors, particularly in what concerns to the reduction of energy consumption and the… Expand

We present a novel weighted Fourier series (WFS) representation for cortical surfaces. The WFS representation is a data smoothing… Expand

AIMS/HYPOTHESIS Mutations at the gene encoding wolframin (WFS1) cause Wolfram syndrome, a rare neurological condition… Expand

Wolfram syndrome, an autosomal recessive disorder associated with diabetes mellitus and optic atrophy, is caused by mutations in… Expand

Analysis of drifter trajectories in the Gulf of Mexico has revealed the existence of a region on the southern portion of the West… Expand

In Wolfram syndrome, a rare form of juvenile diabetes, pancreatic beta-cell death is not accompanied by an autoimmune response… Expand

Mutations of the WFS1 gene are responsible for Wolfram syndrome, a rare, recessive disorder characterized by early-onset, non… Expand

Mitochondrial (mt)DNA haplogroups in a German control group (n = 67) were characterized by screening mitochondrial coding regions… Expand