A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

Overview of attention for article published in Nature Genetics, October 1998

Altmetric Badge

About this Attention Score

In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (91st percentile)
Good Attention Score compared to outputs of the same age and source (73rd percentile)

Mentioned by

patent: 5 patents
wikipedia: 4 Wikipedia pages

guideline: 1 clinical guideline source

Readers on

mendeley: 185 Mendeley

So far, Altmetric has seen 4 citations on 4 Wikipedia pages.

English

Wolfram syndrome

Cited by user Nbdo on 29 Jul 2024

Wolfram syndrome, also called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness), is a rare autosomal-recessive genetic disorder that causes…

Catalan

Wolframin

Cited by user BQUB19-Yualex on 25 Oct 2019

Arabic

WFS1

Cited by user JarBot on 14 Jul 2018

English

WFS1

Cited by user ProteinBoxBot on 17 Dec 2007

Wolframin is a protein that in humans is encoded by the WFS1 gene.

This page shows the most recent Wikipedia articles that mention this research output. Click here to find out how to access more activity.